Trade Lead Description:
Osmunda has successfully assisted nearly 1,200 domestic and foreign enterprises in achieving various medical devices registration and certification. We will be your trustful partner and your most professional guide. We can: - analysis of company needs, applicable regulatory and statutory requirements and, where applicable, customer specifications and expectations
- pre-assessment and gap analysis of existing Quality Management System
- design and integration of ISO 13485-compliant Quality Management Systems
- Quality Management System development and implementation action plan
- preparation of Quality Manual, policies, procedures/protocols in line with ISO 13485
- GMP /cGMP- (current) Good Manufacturing Practices requirements
- Document Control, including applicable forms, templates, publications, etc. - Control of Records, Data Management, R&D, manufacturing, shipping, traceability and QA
- research and assistance in preparation of the specifications, procedures and standard
Type of Offer: |
Offer to Sell |
Quantity: |
Not Specified |
Packaging: |
Not Specified |
Price / Incoterms Conditions: |
Not Specified |
Posted from China - Guangdong on 31 July, 2012
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