Global Consultants Serving the Medical Device Industry
Need assistance with your quality system installation, medical device development, or FDA QSR compliance?
GPMG is one of the first consulting firms to combine onsite medical device consulting services with practical industry products. We assist companies at all stages of development, whether they are single medical device start-up or a mature medical device company with multiple product platforms.
GPMG has developed a series of products for the medical device industry to address common areas of need, such as our modular ISO 13485 quality system designed to streamline our clients ISO 13485 quality system certification goals, an FDA 510k regulatory submission template designed to simplify the FDA submission process, several sterile packaging validation protocols, and numerous individual ISO 13485 procedures to quickly address compliance gaps in existing systems.
Therefore, whether it is our FDA QSR ISO 13485 quality system and validation products, our medical device consulting services, or a combination of all of the above GPMG stands ready to assist you, anywhere in the world.
Questions or Comments?
Feel free to call us at 202.380.9380
or email us at email@example.com
GPMG's Modular ISO 13485 Quality System
FDA 510k medical device submissions, medical device process validation, medical device sterile packaging validations, medical device ISO 13485 quality system, medical device FDA QSR compliant quality systems, FDA QSIT audit preparation, FDA consulting, accelerated aging protocols, FDA QSR audits, ISO 13485 quality system certification support, modular iso 13485 quality system product, ISO 13485 quality system procedures