A wealth of expertise in clinical research exists within RegPak BioPharma Consulting. We have extensive experience of the preparation, submission and approval process for clinical trial applications in major clinical trial conducting countries. Our team of experts are in regular agency contact and represent the cutting edge of clinical regulatory affairs. RegPak BioPharma Consulting can offer specialized consultancy advising on clinical and regulatory strategy for new product development, design of clinical trial protocols and preparation of applications for Clinical Trial Authorizations.
From Discovery to the Pre-Clinical Phase
Our services include
Strategy and Consulting
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Regulatory Affairs
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Pharmacovigilance
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Quality
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Clinical Trial Service
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