Own-Label Manufacturer
State License Servicing offers tailored pharmaceutical licensing and compliance support for own-label distributors and virtual manufacturers. Our experienced regulatory team, relying on human intelligence rather than AI, handles state-by-state filings, renewals, change noticing, and ongoing compliance so you don’t have to.
We track regulatory changes in real time and ensure your licenses remain current across all U.S. jurisdictions, helping you avoid costly delays or disruptions. With SLS managing the regulatory burden, you can focus on growing your brand and delivering quality pharmaceutical products to market with confidence.
State License Servicing offers a range of services to help manufacturers operate efficiently and in compliance with regulations, including:
Full Service White Glove State License Portfolio Management
Do you know the drug and device distribution laws in all 50 states, DC, Guam and Puerto Rico?
SLS does! Whether you’re a virtual manufacturer leveraging 3PL services or a company self-distributing your own label, we’ve got you covered.
SLS takes on the responsibility of managing your license portfolio, from initial applications and renewals to any required change notifications.
Our team ensures you stay licensed and operational without disruption, so you can focus on growing your business. We manage the intricate details of compliance, so you can confidently stay in business, ship your products, and avoid costly penalties.
We take care of the regulatory compliance, so you can stay focused on your core business.
PharmaRegsᴴᴵ Subscription Software
Staying licensed is staying in business.
Puerto Rico Services
If you’re a drug manufacturer distributing into Puerto Rico, compliance starts with two key requirements: registering your products with the Puerto Rico Department of Health (PR DOH) and appointing a local representative agent. We serve as your trusted on-island partner with owned, staffed offices in Puerto Rico, ensuring you meet all regulatory obligations with speed and accuracy. We manage the full product registration process, maintain your active licenses, and act as your official liaison with PR DOH and the Pharmacy Board.
Are you a device manufacturer? The PR DOH is preparing to implement registration requirements for all medical devices not containing a drug. Now is the time to prepare and we’re ready to help you stay ahead.
With our team on the ground and compliance expertise on your side, you’ll have confidence that your Puerto Rico operations are fully covered.
Drug Price Transparency Reporting
Drug Price Transparency Reporting Made Easy for Label Owners
Navigating state drug price transparency laws can be time-consuming and costly for drug label owners, especially with multiple states requiring detailed, ongoing disclosures. That’s where we come in.
Our State DPT Servicing team manages every aspect of drug price transparency reporting on your behalf, including initial data submissions, pricing change notifications, and continuous compliance monitoring. We ensure you’re always up to date with the latest state-specific regulations, deadlines, and platform updates. By utilizing our specialized team focused on pharmaceutical reporting, you not only reduce compliance risks and avoid costly penalties, but also free up your internal resources to focus on what truly matters – business growth and innovation.
Let us handle the complexity, so you can focus on your business.
NABP Drug Distributor Accreditation
Accreditation Starts with Preparation.
Securing Drug Distributor Accreditation through the NABP is a vital step for manufacturers, whether you self-distribute or depend on logistics partners, to ensure national compliance. Achieving this accreditation requires thorough preparation to align your operations and Standard Operating Procedures (SOPs) with the rigorous standards set by the NABP.
Our team supports you through every stage of this process by reviewing your facility, processes, and documentation. We help identify areas for improvement, ensuring that your business not only meets but exceeds the necessary requirements.
With our assistance, you can confidently navigate the accreditation process and prepare for a smooth, successful inspection.
Trust in our expertise to help you achieve and maintain accreditation.
DSCSA Compliance Through Trading Partner Verification Services
ToVerify: Trading Partner Verification Made for Today’s Supply Chain
Under the Drug Supply Chain Security Act (DSCSA), manufacturers are responsible for verifying the licensure and credentials of all trading partners, not just those receiving shipments. That’s where ToVerify comes in. ToVerify provides end-to-end verification of state licensure and federal distribution credentials for both drug and device partners, ensuring full compliance with DSCSA requirements. This is especially critical for virtual manufacturers using third-party logistics (3PL) providers, as most 3PLs can only validate ship-to locations, not upstream or downstream trading partners.
With ToVerify, you gain confidence that every trading partner in your network is properly licensed and verified – protecting your company from compliance gaps and regulatory risk.
Industry Compliance Updates
Stay Ahead of the Curve in a Changing Regulatory Landscape.
Manufacturers face constant pressure to keep up with evolving state licensing laws and regulatory changes. Our Industry Compliance Updates deliver timely, accurate insights that help you avoid surprises, reduce risk, and make informed decisions.
With concise, easy-to-digest summaries of relevant updates based on your specific operations, your team can focus more on production and less on regulatory guesswork.
Whether it’s a new licensing requirement or a revision to an existing rule, you’ll know what’s coming and how to stay compliant.
These updates are curated to support operational efficiency and protect your business from costly compliance lapses.
Turn regulatory complexity into a competitive advantage.
Why we are different
State License Servicing provides expert pharmaceutical licensing and compliance services, without relying on AI.
Unlike AI tools that miss updates, misinterpret state regulations and are simply confined by the design of a board’s website, our legal and compliance departments use human intelligence, not AI, to deliver accurate, vetted human-driven support. We help drug and device manufacturers stay compliant with evolving state licensing regulations, offering tailored solutions based on real-time oversight and direct personal engagement with each state board.
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