D.O.C. S.r.l. - Documentation Organization and Consultancy

Your Partner in GMP Compliance

General Information
Company Name
D.O.C. S.r.l. - Documentation Organization and Consultancy
Founded Year
1997
Location (Offices)
Italy +2
Founders / Decision Makers
Number of Employees
47
Industries
Health Care, Manufacturing, Pharmaceutical
Funding Stage
-
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D.O.C. S.r.l. - Documentation Organization and Consultancy - Company Profile

D.O.C. S.r.l. - Documentation Organization and Consultancy is an Italian consulting company specializing in cGMP Compliance & Validation for the pharmaceutical industry. Founded in 1997, the company has gained international experience and expanded its services over the years to cater to pharmaceutical companies and their suppliers, including engineering and contracting companies and original equipment manufacturers. The company's core business involves acting as a "System Integrator" and "Communication Platform & Facilitator" to ensure the compliance of pharmaceutical systems with cGMP requirements, resulting in fully validated and functional systems. In 2014, D.O.C. opened a new headquarters to accommodate training sessions and seminars, demonstrating its commitment to meeting market demands. Its service portfolio encompasses equipment and system qualification & validation, instrumentation calibration & maintenance, product & process validation, and cGMP consultancy and training. The company's operations are inspired by the GMP V-model Validation Life Cycle, ensuring full traceability and documented evidence throughout the process. D.O.C.'s focus on the qualification of pharmaceutical facilities and the compliance of pharmaceutical manufacturing processes positions it as a critical player in the industry. With a website (www.docvalidation.it) offering further details, the company is well-poised to continue its growth and play a significant role in shaping the future of pharmaceutical compliance and validation.

Taxonomy: cGMP Compliance, Validation Services, Consultancy, Equipment Qualification, System Validation, Process Validation, Product Validation, Instrumentation Calibration, Maintenance Services, Pharmaceutical Manufacturing, Training Services, System Integration, User Requirement Definition, Traceability Management, Documented Evidence

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