A New Year, A New Federal Market: Kicking Off 2026 at the Winter Training Conference
Happy New Year! As we begin 2026, the federal procurement landscape continues to evolve. With major acquisition reforms underway, the year ahead will be pivotal for the federal acquisition community.
The Coalition for Common Sense in Government Procurement’s Winter Training Conference: The Revolutionary Federal Market is designed for acquisition professionals to start the year with clarity and insights. With the conference less than two weeks away, the January 14–15 event will bring together government leaders and industry experts to examine what’s next for the federal market and what that means for businesses. Learn more about the excellent agenda below, and be sure to register!
To register, click here. For questions or assistance with registration, please contact Madyson Whiting at mady.whiting@thecgp.org. Please use the link to secure your room in our block at the discounted rate: Book your group rate for CGP Conference
Day One: Governmentwide Focus
The Honorable Dr. Kevin Rhodes, OFPP Administrator
Day One of the Winter Training Conference explores key governmentwide issues shaping the federal acquisition system, including major policy reforms and acquisition modernization efforts.
The day will begin with opening remarks from GSA Acting Deputy Administrator Mike Lynch, followed by an acquisition panel featuring Larry Allen, Associate Administrator of GSA’s Office of Government-wide Policy, and Laura Stanton, Deputy Commissioner of the Federal Acquisition Service.
Our Keynote will feature The Honorable Dr. Kevin Rhodes, Administrator of the Office of Federal Procurement Policy (OFPP), offering a governmentwide perspective on acquisition policy and reform.
Day One sessions will explore major developments shaping the broader federal procurement ecosystem, including:
- The Revolutionary FAR Overhaul – What’s Next?
- GSA’s Consolidation Action Plan
- Updating MAS Ordering Guidance to Support FAR Overhaul Enhancements
- The New IT GWAC Market
- Integrated Award Environment (IAE) / SAM.gov
- The New Schedules Market: Transactional Data Reporting and More
View the full Day One agenda here.
Day Two: Healthcare Focus
Howard Manuel, Deputy Senior Advisor to the Secretary of Veterans Affairs
Day Two shifts focus to the federal healthcare market, with speakers from the Department of Veterans Affairs and Defense Health Agency.
The day will feature a Luncheon Address from Howard Manuel, Deputy Senior Advisor to the Secretary of Veterans Affairs, followed by panels and discussions with senior acquisition leaders and subject matter experts.
Topics on Day Two include:
- VA Acquisition Leadership
- Federal Budget and Legislative Updates
- Impacts of the Revolutionary FAR Overhaul on Federal Healthcare Contractors
- VA Medical/Surgical Prime Vendor Program
- DHA Pharmaceutical Program
- VA Federal Supply Schedule (FSS) Program
- VA Pharmacy Program
- VA Community Care Program
View the full Day Two agenda here.
As agencies continue to implement acquisition reforms, the Winter Training Conference offers a timely opportunity to hear directly from government leaders, understand what’s coming next, and engage with peers across the acquisition community.
As we begin the new year, the Coalition wishes you a happy and successful 2026, and we look forward to welcoming you to the Winter Training Conference as we start the year together.
Thank You, Winter Training Conference Sponsors!
Help Spread the Word! Winter Training Conference Social Media Kit Available
As we count down to the 2025-2026 Winter Training Conference, we are excited to launch our official Social Media Kit to help you spread the word! All attendees can now download customizable graphics and sample posts to share your involvement in this important event.
Let your network know you will be joining the conversation on what’s next for the federal market by using the hashtag #CGPWinter2026.
Download the Social Media Kit here.
Department of War Issues 31 DFARS Deviations Under FAR Overhaul
The Department of War (DoW) has issued 31 deviations to the Defense Federal Acquisition Regulation Supplement (DFARS) as part of the ongoing Revolutionary FAR Overhaul (RFO). The deviations, along with accompanying line-out documents, are available on the department’s website and will take effect February 1, 2026.
The deviations span a wide range of DFARS parts, including:
201, 203, 205, 206, 207, 210, 211, 212, 213, 214, 217, 218, 223, 224, 226, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 239, 240, 244, 248, 249, and 250.
John M. Tenaglia, Principal Director of Defense Pricing, Contracting, and Acquisition Policy, issued a memo announcing the deviations. The memo notes that the remaining DFARS parts should be published by the end of this month (January 2026).
Army to Move Forward with MAPS Contract
The United States Department of the Army announced that it will move forward with the Marketplace for the Acquisition of Professional Services (MAPS) contract.
MAPS will consolidate ITES-3S and RS3 into a single, Army-led professional services vehicle with a 10-year period of performance and a $50 billion ceiling, covering a broad range of IT, engineering, and mission support services.
The Army Contracting Command recently announced its decision to proceed, and an industry day is scheduled for January 28 at Aberdeen Proving Ground to discuss next steps.
GSA Projects Nearly $1B in Savings from Deregulatory Actions
A recent General Services Administration (GSA) news release announced that the agency expects to save nearly $1 billion over the next decade as a result of deregulatory actions completed in 2025. The effort was led by GSA’s Office of Government-wide Policy (OGP) and carried out in support of the Administration’s deregulatory executive orders (EO), including EO 14192, Unleashing Prosperity Through Deregulation, and EO 14219, Ensuring Lawful Governance and Implementing the President’s “Department of Government Efficiency” Deregulatory Initiative.
According to GSA, the initiative focused on eliminating outdated and duplicative regulations, ending diversity, equity, and inclusion (DEI) programs and preferences, and promoting greater efficiency across Federal operations. As part of this effort, GSA eliminated 72 percent of the Federal Management Regulation (FMR) and 50 percent of the Federal Travel Regulation (FTR) following a comprehensive review by OGP’s Office of Asset and Transportation Management. GSA also removed 84 regulatory bulletins totaling more than 96,000 words and 194 pages from the Federal Register. The agency estimates that the elimination of these bulletins alone will generate $19.3 million in savings over ten years. GSA noted that, where appropriate, it will issue non-regulatory guidance to agencies to reduce regulatory burden.
“This represents one of the most significant deregulatory achievements in GSA’s history,” said Larry Allen, Associate Administrator of OGP. “By eliminating outdated and unnecessary requirements while maintaining statutory compliance, we’re delivering real savings to taxpayers and removing barriers to efficient government operations.”
GSA Withdraws Planned Layoffs Within Technology Transformation Service
Government Executive reports that GSA has rescinded notices previously sent to employees within its Technology Transformation Service (TTS) indicating a potential reduction in force (RIF). The notices, issued in April, would have affected staff in the Office of Awards, Regulatory, and Oversight Systems, as well as portions of the Digital Services Division.
TTS oversees several governmentwide technology initiatives, including Login.gov, the Federal Risk and Authorization Management Program (FedRAMP), and Cloud.gov. According to the report, the decision to rescind the notices was driven in part by provisions in the current Continuing Resolution, which prohibit Federal agencies from initiating or carrying out RIFs through January 30.
A recent GSA Office of Inspector General (OIG) report found that TTS staffing levels are already down 67 percent compared to January 2025 and identified staffing challenges as the agency’s most significant risk heading into 2026. The report also noted that GSA has reduced its information technology workforce by approximately 40 percent this year.
TTS Director Thomas Shedd reportedly told employees that the service will reassess its workforce needs and any potential future staffing actions after January 30.
Testimony Provides Insights into VA’s Planned 2026 EHR Expansion
Federal News Network reports that the Department of Veterans Affairs (VA) plans to resume expansion of its Electronic Health Record (EHR) system using a batch deployment approach beginning in 2026. Dr. Neil Evans, Acting Program Executive Director of the VA’s EHR Modernization Integration Office, recently testified before the House that the department intends to bring the system live at 13 additional locations next year, with the first sites scheduled to go live in April 2026.
According to Dr. Evans, the VA plans to deploy the EHR system at multiple facilities simultaneously within each wave in an effort to accelerate implementation and improve coordination across sites. The strategy reflects lessons learned from earlier deployments, which have faced operational and usability challenges.
VA’s EHR system is currently operating at six locations nationwide. Full deployment would require implementation at an additional 164 sites, for a total of 170 facilities. Dr. Evans testified that the VA could complete nationwide deployment as early as 2031. The VA paused EHR deployments in April 2023 to address persistent outages and usability issues reported by medical staff at facilities already using the system.
FDA Explores New Contracting Model to Support Public Health Innovation
The Food and Drug Administration (FDA) recently issued a Request for Information (RFI) seeking input on a potential new contracting approach that would allow the agency to collaborate more directly with venture capital firms and their portfolio companies. According to the RFI, FDA is exploring a contract model that would establish direct relationships with qualified venture capital firms, allowing companies within an approved firm’s portfolio to compete for and receive task orders.
FDA notes that many emerging technologies relevant to its public health mission, such as artificial intelligence, biotechnology, medical devices, and regulatory technology, are being developed by companies backed by venture capital firms. The agency is examining whether a revised contracting approach could help improve access to these innovations. Responses to the RFI are due by 2:00 PM (ET) on January 18, 2026.
Off the Shelf: A NASA SEWP Update
Joanne Woytek, NASA SEWP Program Director, joined Off the Shelf to discuss the performance of the NASA SEWP V contract over the past decade.
During the interview, she provided an overview of the program’s key metrics, including customer profile, current year and overall performance, types, and scope of mission support for customer agencies.
Woytek also discussed the role of data, explaining how NASA SEWP supports customer agencies through procurement data collection and analysis, and she gives an update on NASA SEWP VI. The evolution of technology and the NASA SEWP approach to meeting customer needs are another discussion topic.
Finally, Woytek shared her thoughts on the keys to management success in leading the program for over two decades.
Listen to the full interview here.
Updated FY25 VA Data Sets Now Available for Members
To increase the number of valuable tools available for members, the Coalition has compiled several data sets pertaining to VA Medical Centers’ procedures, diagnoses, and product spend. Data through FY25 is now available. Below is a description of the VA data reports that the Coalition can provide to healthcare members based on areas of interest to their business:
- Diagnosis data by each VA Medical Center: Members can request a report by providing the relevant International Classification of Diseases (ICD-10) codes of interest.
- Procedure data by each VA Medical Center: Members can request a report by providing the relevant Current Procedural Terminology (CPT) codes of interest.
- Prosthetic (medical implants, DME) product spend by VA Medical Center: Members can request a report by providing the relevant Healthcare Common Procedure Coding System (HCPCS) codes for items managed by VHA Prosthetics.
- VAMC Surgeries: A report detailing total surgical procedures performed at individual VA Medical Centers.
- Total Veterans Health Administration (VHA) Surgeries: A systemwide summary of surgical volume across the entire VHA.
For any data requests or related questions, please contact Michael Hanafin at mhanafin@thecgp.org.
Reminder: OFPP Seeks Public Input for Next Phase of FAR Overhaul
The RFO is moving into its next phase in 2026, and the Office of Federal Procurement Policy (OFPP) is seeking broad public input to help shape it. To support this effort, OFPP has launched a new IdeaScale community designed to collect feedback from the acquisition workforce, industry, and other stakeholders on ways to streamline and modernize the FAR.
Through the platform, participants can submit ideas on practices agencies should start, stop, or refine as the government works toward a rewritten and simplified FAR. Community members may also view, comment on, and vote for ideas posted by others, helping OFPP identify the most impactful recommendations.
OFPP describes this as a key opportunity to contribute to a “historic initiative” that aims to reset the foundation of federal buying. The IdeaScale community will accept feedback through January 12, 2026.
Legal Corner: U.S. House Passes FY 2026 NDAA that includes BIOSECURE
The Legal Corner provides the procurement community with an opportunity to share insights and comments on Legal issues of the day. The comments herein do not necessarily reflect the views of The Coalition for Common Sense in Government Procurement.
Authored by Joy E. Sturm, Allison D. Pugsley, Tim Bergreen, Michael N. Druckman, and Ajay Kuntamukkala; Hogan & Lovells
The final FY 2026 National Defense Authorization Act (NDAA) was released on December 7, inclusive of a modified version of the Senate-passed BIOSECURE Act from October. This final bill maintains the core structure of the Senate’s BIOSECURE text while making several targeted changes. Congress has kept the government-wide prohibition concept intact, while closing a “gap” that could have resulted in federal health program impact, limiting the scope of coverage, narrowing the “knowledge” requirement, and reducing potential operational friction in areas like overseas health care.
In terms of timing, the NDAA is on a relatively fast track to become law. The House of Representatives passed the NDAA on December 10. The Senate is expected to pass the NDAA during the week of December 15. The White House has issued a formal Statement of Administration Policy supporting the NDAA, stating that the President will sign the NDAA into law when it is presented to him for signature. Depending on exactly when the Senate passes the NDAA, President Trump is expected to sign the NDAA into law either during the week of December 15 or the following week.
The basic structure of BIOSECURE remains the same from the version included in the Senate-passed NDAA: executive agencies will be barred from procuring biotechnology equipment or services from “biotechnology companies of concern” and from entering into contracts performed using such equipment or services. Related prohibitions will apply to certain grants, loans, and cooperative agreements.
The term “biotechnology companies of concern” continues to include 1) companies on a list to be published by the Office of Management and Budget (“OMB”), as well as 2) companies included on Department of Defense/War (“DoD”)’s Section 1260H list of Chinese military companies. OMB remains responsible for establishing and managing an interagency process to identify biotechnology companies of concern, maintaining and updating a public list, and coordinating with the Federal Acquisition Regulation (“FAR”) Council on necessary changes to procurement regulations.
Passage and enactment are virtually certain. Once the NDAA is signed, OMB will need to establish the designation process, consult with national security and health agencies on criteria and specific entities, and coordinate with the FAR Council on regulatory execution.
Some noteworthy changes in the final bill:
- First, the conference text narrows the automatic capture of entities on DoD’s Section 1260H list of Chinese military companies. Under the Senate version, 1260H status alone effectively made a firm a biotechnology company of concern, even if the firm in question had no connection with biotechnology. The final bill now requires a biotechnology nexus: a 1260H-listed entity must also be involved to some extent in manufacturing, distributing, providing, or procuring biotechnology equipment or services. Recent news reports indicate that a Pentagon roster of companies to be added to the 1260H list in the next update includes WuXi Apptec.
- Second, affiliates of companies of concern are no longer “automatically” covered by BIOSECURE by virtue of their relationship to a covered company. The earlier Senate text had pulled in any subsidiary, parent, affiliate, or successor of a covered entity as a “biotechnology company of concern,” so long as it met only the “foreign adversary governance/control” criterion. The final bill drops the term “affiliate” entirely and only captures affiliates that are parents, subsidiaries, or successors. And these entities must meet the full set of criteria that apply to directly designated entities, including both the foreign adversary nexus and the specific biotechnology and national security risk factors.
- Third, the scienter standard for contractors is narrowed to require actual “knowledge.” The Senate-passed and earlier versions of the BIOSECURE bill broadly covered contractors that would “know or have reason to believe” that performance of a federal contract would require the use of prohibited biotechnology equipment or services. The final bill pares the restriction back to contracts that the contractor “knows” will require such use, a change that is no doubt welcome to contractors who may not have full visibility of relevant supply chains.
- Fourth, the final bill addresses potential Federal health program impact. We had flagged in our October 25, 2025 alert that although BIOSECURE applies only to federal procurement contracts, and not to reimbursement/payer contracts such as those supporting federal health programs, the bill could have “collateral” federal health program impact on pharma/biotechnology manufacturers supplying BIOSECURE-restricted product. The final text attempts to protect manufacturers from this impact by providing that a company will be deemed to be in compliance with its statutory requirement to make product available for procurement on Federal Supply Schedule contracts, and thus not blocked from Medicare Part B and Medicaid, if the Secretary of VA determines that the company “would comply” with the statutory requirement but for the prohibitions of BIOSECURE.
- Fifth, the final bill clarifies a politically sensitive topic: overseas health care for U.S. government personnel and their families. The earlier Senate-passed bill excepted U.S. employees and uniformed service members whose official duty stations are overseas, as well as certain contractor employees supporting them. The final bill expands that carve-out to explicitly include dependents, TRICARE-covered beneficiaries, and other categories of beneficiaries for whom care is provided by a U.S. department or agency, while maintaining the contractor-employee component.
A January 7, 2025, Federal Register Notice (“90 FR 1105) regarding additions to the 1260H List also published the Reconsideration Process. Entities on the 1260H List seeking reconsideration must submit the following information to DoD:
- Entity Information:
- The listed entity’s name and mailing address (including email address).
- An authorized representative’s name and mailing address (including email address).
- Statement of Reconsideration:
- A statement indicating the entity’s intent to request reconsideration of the Department’s determination.
- A detailed description, supported by evidence, explaining why the entity should be removed from the 1260H List.
- Additional Information:
- Arguments and evidence that demonstrate either 1) an insufficient basis for the listing, or 2) that the circumstances leading to the listing no longer apply.
We note, as a final point, that the timing profile is adjusted at the margins. BIOSECURE prohibitions still do not take effect until after OMB has acted and the FAR Council has amended the regulations. However, in the earlier Senate-passed version, the non-1260H entities added through the OMB process did not become subject to the procurement ban until 180 days after the FAR revisions. The final bill shortens that period to 90 days. For 1260H companies, the FAR implementation period of 60 days has not been revised.
Next steps
If you have questions or would like to discuss, please reach out to our BIOSECURE team: Joy Sturm, Allison Pugsley, Timothy Bergreen, Mike Druckman, Ajay Kuntamukkala, Ari Fridman, Cybil Roehrenbeck, Ashley Roberts, and Ashley Ruhe.
VA Issues MSPV Solicitation, One-on-One Meetings at the Winter Training Conference
Yesterday, the VA Medical/Surgical Prime Vendor (MSPV) team released the updated solicitation for consumable commodities in support of the MSPV program catalogue. Offers are due on January 19, 2026 at 5 PM (ET).
We are excited to share that the VA MSPV program team will hold one-on-one meetings with attendees on Wednesday, January 14 (governmentwide day) as part of the 2025-2026 Winter Training Conference. To schedule a 15-minute meeting, please reach out directly to the appropriate contact. Meetings will be scheduled on a first-come/first-served basis.
A list of all available VA representatives, along with their contact information, is provided below.
If you have not yet registered for the Winter Training Conference, you may do so here. Please note that conference registration is required in order to participate in the one-on-one meetings.
Med/Surg Supply BPA One-on-One Meetings: January 14 (Day One of the Conference)
Jeremy Boston: Jeremy.Boston@va.gov
Pedro Jaime Catinchi: Pedro.CatinchiJaime@va.gov
Brett Cook: Brett.Cook@va.gov
Katherine Corcoran: Katherine.Corcoran@va.gov
Jon-Paul Grizzle: Jon-Paul.Grizzle@va.gov
Edward Lyke: Edward.Lyke@va.gov
Crystal Martin: Crystal.Martin5@va.gov
Matthew McDonell: Matthew.McDonell@va.gov
Princess Mersha: Princess.Mersha@va.gov
Jeremy Parker: Jeremy.Parker2@va.gov
Michael Pierson: Michael.Pierson@va.gov
Sarah Scott: Sarah.Scott1@va.gov
Melanie Stockman: Melanie.Stockman@va.gov
Rashaun Thomas: Rashaun.Thomas@va.gov
If you have any questions, please contact Michael Hanafin at mhanafin@thecgp.org. We look forward to seeing you at the conference in January!
Register for the Small Business Summit! Jan. 13
On January 13, the Coalition will host its third annual Small Business Summit, a half-day forum featuring key insights and analyses into the latest developments regarding small business policy, subcontracting, teaming, joint venture agreements, and more.
The program will consist of valuable sessions featuring experts from government and industry, and the chance to network with peers in the procurement community. The Summit is an excellent opportunity for both small and large businesses to increase their knowledge about small business policy and what makes for a successful, sound business relationship.
Small Business Administration (SBA) Regulatory Update
John Klein, SBA Deputy General Counsel, will provide a Regulatory Update, giving key insights into recent and upcoming regulatory changes impacting small businesses. Attendees will be informed on the latest SBA policies and how they affect compliance and opportunities in federal contracting.
Small Business Subcontracting
The Summit also features a panel on small business subcontracting, with perspectives and insights from large and small businesses. Speakers will discuss compliance considerations, opportunities, and practical strategies for building successful partnerships in today’s federal marketplace. Attendees will gain a clearer understanding of how primes and subs can work together to meet subcontracting goals and deliver best value to government customers.
SBA Policies and Programs Update
Finally, there will be an update on the latest SBA government contracting programs and policies. Experts will review recent regulatory developments, upcoming changes affecting small business eligibility and certifications, and new tools and initiatives designed to support small businesses.
This event is complimentary to all Coalition members, and both in-person and virtual attendance are available! Register here. For any assistance, please contact Madison Whiting at mady.whiting@thecgp.org.
Webinar – Overview of the NDAA for Fiscal Year 2026, Jan. 22
Join the Coalition and Moshe Schwartz, President of Etherton and Associates, Inc., on January 22 from 12:00 – 1:00 PM (ET) for an Overview of the National Defense Authorization Act (NDAA) for Fiscal Year 2026.
During the webinar, Moshe will highlight trends and focus areas of the NDAA, including:
- Acquisition;
- The Industrial Base;
- Cybersecurity Provisions; and
- More
To register, click here. For assistance with registration, please contact Mady Whiting at Mady.Whiting@thecgp.org.
Webinar – OASIS+ Phase II: New Domains. Continuous Enrollment. Bigger Possibilities, Jan. 27
GSA is set to reopen all six OASIS+ solicitations on January 12, 2026, under a continuous enrollment model—introducing five new service domains that expand the playing field for professional services contractors. This update reflects Executive Order 14240 and GSA’s push to simplify acquisition and consolidate spend.
On January 27 from 12:00 – 1:00pm EST, please Join Leo Alvarez, Principal at Baker Tilly, Dylan Schreiner, Government Contractor Solutions Senior Manager at Baker Tilly, and the Coalition for a practical briefing on Phase II of OASIS+. Leo and Dylan will cover the upcoming pre-amendment notice, draft scorecards, and strategies to position your firm for success.
Topics include:
- The five new domains and their implications;
- Preparing for continuous enrollment; and
- Teaming and qualification best practices.
Whether you’re an incumbent or a newcomer, this session will help you navigate the next chapter of OASIS+.
To register, click here. For assistance with registration, please contact Mady Whiting at Mady.Whiting@thecgp.org.
Webinar – Commerciality Considerations of DoD’s Memo on “Transforming the Defense Acquisition System into the Warfighting Acquisition System,” Jan. 29
On November 7th, the Department of War released a memorandum outlining its initiative to “Transform the Defense Acquisition System into the Warfighting Acquisition System.” Join the Coalition on January 29th from 12:00 – 1:00pm EST for a presentation by Peter Terenzio of Covington and Mike Tomaselli of Chess Consulting as they examine the memo’s major themes and the implications for government contractors.
The session will include a focused discussion on the regulatory framework governing commercial contracting, given the memorandum’s emphasis on expanding the defense industrial base through a “commercial first” strategy. Topics will include:
• Key themes and objectives identified in the memo;
• FAR Part 12 vs. FAR Part 15 (commercial vs. negotiated acquisitions);
• Definitions of commerciality under FAR 2.101;
• Commercial item determinations and DCMA’s role; and
• Alignment with the FAR Overhaul and proposed CAS changes.
To register, click here. For assistance with registration, please contact Mady Whiting at Mady.Whiting@thecgp.org.
2025 Small Business Regulatory Year in Review, Feb. 4
The Coalition will host a virtual 2025 Small Business Regulatory Year in Review presentation on February 4 from 12:00-1:00 PM (ET)! The event features industry experts David Black, Partner at Holland and Knight, Ken Dodds, Vice President of Acquisition Policy at The Coalition for Common Sense in Government Procurement, and Jon Williams, Partner at PilieroMazza, who will provide insights on the regulatory cases and updates of the past year that affected both large and small business contractors.
During the event, Black, Dodds, and Williams will cover a wide range of topics, including observations on:
- Small Business Administration (SBA) updates;
- Office of Hearings and Appeals (OHA) cases;
- Government Accountability Office (GAO)/Court of Federal Claims (COFC) decisions;
- And More
Small and large businesses are encouraged to attend. If you have any questions in advance of the event, please contact Joseph Snyderwine at Jsnyderwine@thecgp.org.
To register, click here. For assistance with registration, please contact Mady Whiting at Mady.Whiting@thecgp.org.
GSA Contract Management Best Practices, Feb. 5
Join us on Thursday, February 5, 2026, from 12:00 – 1:00 PM ET for an insightful webinar on GSA Contract Management Best Practices, led by Sergey Bogol, VP of GSA Contract Management Operations at Price Reporter.
With over 20 years of hands-on experience in supporting GSA contractors, Price Reporter experts will share strategies that successful contractors use to grow and thrive in their GSA business as we move into 2026. In this webinar, Sergey will provide you with a practical contract management playbook centered on repeatable routines designed to protect your contracts and enhance performance. Their playbook is founded on three core pillars that ensure long-term success with GSA:
- Best Practices for Compliance: Learn how to maintain compliance effectively.
- Strategies for Business Growth: Discover ways to expand your business with government contracts.
- Automation and Scaling Techniques: Find out how to automate processes for next-level growth.
Don’t miss this opportunity to elevate your GSA contract management skills!
To register, click here. For assistance with registration, please contact Mady Whiting at Mady.Whiting@thecgp.org.
Earn Conference Discounts through the Member Referral Program!
The Coalition for Government Procurement is excited to offer our Member Referral Program!
For each new member your organization refers, and then joins the Coalition, you’ll receive a $250 discount toward registration for either the Spring or Fall Training Conference. There’s no limit to how many discounts you can earn!
Start referring today to enjoy the rewards while helping expand the Coalition’s membership base and advancing our mission of promoting common-sense procurement.
To make a referral or if you have questions about the program, please contact Heather Tarpley, Vice President of Business Development & Sales, at HTarpley@thecgp.org.
Thank you for being a valued member of the Coalition. Your support is key to our success!