APAC FDA Consulting Services & Solutions
Systems Evaluation

Clients frequently turn—and return—to APAC FDA Consulting for world-class evaluations of their R&D systems, manufacturing systems and processes, and quality control/assurance systems. Just as important, they trust APAC FDA to make powerful, effective recommendations for enhancing current systems and processes.
APAC FDA recognized experts in R&D and manufacturing systems assessments routinely assist clients in:
>> Implementing quality by design for successful commercialization
>> Analyzing and managing risk in the R&D and manufacturing environments
>> Developing requirements and performing audits for clinical material GMP (Phases I, II, and III)
>> Assessing and streamlining development practices
In the realm of quality control and quality assurance systems, APAC FDA consultants are the “go-to” people when needs include:
>> Assessing and managing risk vis-à-vis quality systems
>> Evaluating and enhancing quality unit roles and responsibilities
>> Assessing and improving facilities and equipment systems, materials systems, production systems, and laboratory controls systems