Contract pharmaceutical analysis services to support research and development (R&D), regulatory submissions, GMP production, and post-market requirements.

Pharmaceutical research contract services will help you with your production and GMP manufacturing processes. Concerns regarding drug safety, expensive development projects, complicated manufacturing, consumer demands for evidence-based data, and increased regulatory requirements are all problems that can be solved by gaining a greater understanding of your drug material, drug product, or manufacturing method, which can only be accomplished through experienced analytical studies and detailed analytical data.

While your company concentrates on its core business objectives, you’ll need to find a contract analytical services partner with a track record of consistently high-quality regulatory compliance testing. From the early stages of production through manufacturing and post-marketing analytical support, our contract research services are centered on supporting product development, GMP manufacturing, and distribution.

We can help you accelerate the production process, obtain the right data to complete marketing authorisation submissions, and support your post-marketing requirements with our specialist pharmaceutical research capabilities for diverse products such as biopharmaceuticals, oligonucleotides, inhalation drug products, medical devices, vaccines, and regenerative medicines. We provide Total Quality Assurance expertise to help you achieve and surpass quality, safety, and regulatory requirements by bringing quality and safety to life.