Pharmaceutical Development Services Ltd (PDS) advises on drug development, production strategy and regulatory control of new and existing pharmaceutical products, identifying the current standards for your development regulatory submissions and explaining what must be done to successfully meet the requirements. Our specialised services include:
Regulatory affairs and borderline substances
Chemistry, Manufacturing and Controls (CMC)
API and general chemistry support of drug development
Supply chain management
Quality managements systems
Supply chain GMP compliance
Active substance (API) sourcing and development
Building design and validation
Medical device registration
Pharmaceutical Development including small scale formulation
Training services
Quality services and QP services
Technical Due Diligence
Technology transfer
Expert Witness services
Regulatory affairs and borderline substances
Chemistry, Manufacturing and Controls (CMC)
API and general chemistry support of drug development
Supply chain management
Quality managements systems
Supply chain GMP compliance
Active substance (API) sourcing and development
Building design and validation
Medical device registration
Pharmaceutical Development including small scale formulation
Training services
Quality services and QP services
Technical Due Diligence
Technology transfer
Expert Witness services
Location: United States, West Virginia, Nottingham