PharMed Management Group Inc. offers assistance and advice in the areas of Quality Systems and Regulatory Affairs in the Medical Devices, Pharmaceutical and Biologics Industries.
PharMed Management Group Inc. is a quality, regulatory and compliance expert group, with 12+ years of experience; known for resolving FDA related issues on a timely basis. We are a customer focused, full-service consulting company.
Successful in preparing firms for a FDA inspection, responding to FDA-483, and initiating a Corrective Action Master Plan.
Our clients include US and International medical device, biological, and pharmaceutical firms. We specialize in: · Start-ups · Manufacturers of Combination Products · Manufacturers with Contract Manufacturer partnerships · FDA preparation, including FDA Pre-Approval (PAI) or Post Approval Inspections · Mergers and Acquisitions
We work closely with our clients throughout the duration of their projects. We plan, manage, and track the projects progress in order to meet scheduled completion dates and maximize outputs.