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MCS manufactures IMPs for pre-clinical studies, allowing for the manufacture of small, non-GMP batches. We manufacture nearly every traditional dosage form available on the market today, with a focus on oral, parenteral and topical forms. Our Qualified Personnel, provides you in-house with pharmaceutical documentation essentials on which future GMP manufacturing processes can be easily transferred to. Accompanying your large scale production process, our Qualified Personnel is happy to perform external audits on your behalf.
Analytical development is a continuing, parallel process throughout the diverse product development stages. In a word, MCS will additionally provide you relevant analytical data and certificates - whenever desired or legally required.
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