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Our services
MHRA-licensed site operating to good manufacturing practice (GMP) regulations...
"We were instantly impressed with the approachable, friendly and knowledgeable nature of the team at SCM Pharma. When the project faced challenges, their team kept us informed and up-to-date with the status of the project timelines.The products delivered were great and overall, we had a very positive experience dealing with SCM Pharma." Ian Pardo Quality Assurance Manager (Clinical Biomanufacturing Facility), University of Oxford
formulation clinical trials Commercial
Quality

Quality is the bedrock of our business. Through highly trained and motivated staff working within the embedded quality systems, our aim is to provide the right quality products in a time frame that meets your needs. Complying with current GMP regulations at all times, we monitor our quality performance at monthly review meetings and at board level. We embrace continuous improvement and are ever watchful of tools and techniques that can enhance our quality performance. We have trained out and implemented human error risk reduction techniques and risk analysis methodology across the site.

We work in partnership with our clients to help your IMP project move forward. Initially, a Technical Agreement will be signed to ensure that respective responsibilities are understood and documented. A Product Specification File is then prepared and approved ensuring that your IMP requirements are fully met and in compliance with the IMPD/IND. To find out more about our quality systems or to arrange an audit, please get in touch.
 
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