In pharmaceutical development, collaborating with multiple Contract Development and Manufacturing Organisations (CDMOs) and Contract Research Organisations (CROs) poses potential hurdles - from poor communication to delays, errors, and inconsistent feedback during the progression from preclinical to formulation optimisation and clinical trials.

Download our SGS guide to discover:

• How to collaborate in the fast-paced world of drug development
• The current challenges of working with different CDMOs and CROs
• A pathway built to bring drug development consultancy, bioanalysis, formulation and manufacturing, and clinical research services into one program
• How do SGS PACE regulatory consultancy services factor into the mix?

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