Medical Device and Pharmaceutical Drug Manufacturing Consultants

M e n t o r

Documents and Consulting

21 CFR 820 and ISO 13485:2016 Quality Systems Management

Services

Audit Preparation, Internal Auditing
Regulatory Compliance
Project Management
Quality Assurance
Quality Control
21CFR 820
ISO 13485: 2016
Validation Engineering
Disparity Studies
Computer Systems Assurance
IT Systems Validation

Data Analytics
FDA Remediation Projects
GMP, GLP, GDP, GxP
21CFR parts 210, 211
CAPA
Deviation Management
Training
COFEPRIS Compliance
Audit Hosting

Mentor Documents and Consulting offers your organization:

Our team offers an extensive wealth of knowledge that will be invaluable to keep your company stay up to date with new regulations, enforcement trends and up to the minute industry challenges. Class I, II, and III, Medical Device Experts.

I'm a product description. I'm a great place to add more details about your product such as sizing, material, care instructions and cleaning instructions.

I'm a product

Name: I'm a product
SKU: 21554345656

SKU: 21554345656

$120.00

Quantity

I'm a product detail. I'm a great place to add more information about your product such as sizing, material, care and cleaning instructions. This is also a great space to write what makes this product special and how your customers can benefit from this item.

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Medical Device and Pharmaceutical Drug Manufacturing Consultants

M e n t o r

Documents and Consulting

21 CFR 820 and ISO 13485:2016 Quality Systems Management

Services

I'm a product

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