Services at a Glance
Clinical Research Services (Phase II to Phase IV) to Pharmaceutical/ Biotechnology/ Medical Device Industry.
Representation Services (EAR) from our U.K. office, to Medical Device Manufacturers worldwide against mandatory requirement of European Directive.
MDQMS (Medical Devices Quality Management Services- ISO 13485: 2003)
Product Certification (CE Marking) of Medical Devices
US FDA consulting services to Medical Device Manufacturers
Third party Inspection Services
Services at a Glance
- Clinical Research Services (Phase II to Phase IV) to Pharmaceutical/ Biotechnology/ Medical Device Industry.
- Representation Services (EAR) from our U.K. office, to Medical Device Manufacturers worldwide against mandatory requirement of European Directive.
- MDQMS (Medical Devices Quality Management Services- ISO 13485: 2003)
- Product Certification (CE Marking) of Medical Devices
- US FDA consulting services to Medical Device Manufacturers
- Third party Inspection Services
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