commercial-legal/IP-Regulatory assessments are taken for-granted. but when it comes to technical activities (viz., GMPs, product specifications, process controls etc.,) no two companies have similar approach!!! ( it could be as simple as validation parameters/criteria or as complicated as specification/controls...!!!)
How much (to what extent) do you ensure the alignment of above areas with your company standards/policies?
How do handle the conflict/alignment with your quality systems/policies.?
How much (to what extent) do you ensure the alignment of above areas with your company standards/policies?
How do handle the conflict/alignment with your quality systems/policies.?