The pharmaceutical compounding industry is an ever-changing regulatory landscape. Pharmacies and outsourcing facilities that choose The cGMP Compliance Group will get to market faster with better outcomes with our robust business planning services.
Cleanrooms must be built or renovated correctly in order to provide safe, high-quality compounded preparations to patients. Hospitals and 503A pharmacies need to meet USP <795>, USP <797> and USP <800> standards while 503B outsourcing facilities must meet CGMP and follow 21 CFR 211. Let The cGMP Compliance Group take the guesswork out of designing a compliant cleanroom facility to produce quality compounds and reduce the potential for contamination.
The cGMP Compliance Group offers leadership solutions for compounding organizations going through dynamic and challenging growth phases.
Our team has been leading hospital, pharmacy, and 503B outsourcing facilities for over 20 years. Our model allows for customizable solutions to be crated around your objectives - from short-term interim roles to annual fractional positions.
Whether you’re in the end-stage development of an exclusive compound or trying to break into a new healthcare specialty, you need the right business strategy to be successful. The cGMP Compliance Group is here to help outsourcing facilities assess the financial, operational, and regulatory factors of compound development. Let us help increase your revenue potential today!
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