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Our services are tailored to meet our Biotechnology, Pharmaceutical and
Medical Device clients needs in a variety of areas, including,
- Quality Assurance (GMP, GLP, GCP, Audits, Compliance)
- Validation (Method, Process, Equipment and Computer/Software, 21 CFR Part 11, 810,820)
- Regulatory Affairs (IND, NDA, BLA submissions)
- IT (IT Compliance, SAS, Bio-informatics)
- Clinical Affairs (Contract Clinical Research Associates, Site
Investigation, Monitoring, Trial Managers)
Akraya Scientific’s mantra is flexibility without sacrificing quality.
Like many of our client organisations, we are nimble enough to be able to move quickly with flexibility. Equally we have sufficient
critical mass in-house to address the in-depth needs of our clients.
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