Established in 1997 DOC is an Italian consulting company with international experience in the cGMP Compliance & Validation for the pharmaceutical industry
Thanks to a constant business increase generation and in order to satisfy the market demand, in 2014 the company opened a brand-new headquarters able to host training sessions and seminars.
DOC core business is mainly addressed to pharmaceutical companies and their suppliers such as Engineering & Contracting Companies and Original Equipment Machine (OEM) manufacturers.
In this working environment, DOC plays for its Clients the role of “System Integrator”, acting as “Communication Platform & Facilitator” between the cGMP Compliance Requirements (the complying of which is the ultimate Target of any Pharmaceutical System) and the Final Users. The result is a totally validated and functional system.
Initially focused on the qualification of pharmaceutical facilities including manufacturing equipment and critical utilities systems, along the years DOC expanded and specialized its service portfolio, currently embracing the full cGMP compliance of pharmaceutical manufacturing processes for any kind of finished drug form like APIs, solid and liquid.
Specifically DOC operations are organized in the following service segments:
• Equipment and System Qualification & Validation
• Instrumentation Calibration & Maintenance
• Product & Process Validation
• cGMP Consultancy and Training
DOC service portfolio is inspired and developed considering the GMP V-model Validation Life Cycle starting from the User Requirement Definition of a new system to the routine Qualification Maintenance of an existing one. Beside, all the activities and services are conducted according to the “Validation Life Cycle Approach” in order to guarantee the full traceability and documented evidence.
For further information, please visit our website: www.docvalidation.it
Company Details
- Employees
- 47
- Founded
- -
- Address
- Viale Delle Industrie 12 Bis, Settala,milan (Italy) 20090,italy
- Industry
- Pharmaceutical Manufacturing
- NAICS
-
Pharmaceutical and Medicine ManufacturingMedicinal and Botanical ManufacturingPharmaceutical Preparation ManufacturingIn-Vitro Diagnostic Substance ManufacturingBiological Product (except Diagnostic) Manufacturing
- Website
- docvalidation.it
- Keywords
- cGMP Compliance, Education and Training, Validation Services, Consultancy, Calibration and Maintenance, Process and Product Validation, Finished Pharmaceutical Drug Product Release, and Primary, Secondary and Tertiary Packaging Material Qualification.
- HQ
- Settala, Milan (Italy)
D.o.c. S.r.l. - Documentation Organization And Consultancy Questions
D.O.C. S.R.L. - Documentation Organization And Consultancy's website is docvalidation.it
D.O.C. S.R.L. - Documentation Organization And Consultancy's LinkedIn profile is https://it.linkedin.com/company/doc-srl
D.O.C. S.R.L. - Documentation Organization And Consultancy has
47 employees.
View email and phone details for 47
employees at D.O.C. S.R.L. - Documentation Organization And Consultancy.
D.O.C. S.R.L. - Documentation Organization And Consultancy's industry is
Pharmaceutical Manufacturing
D.O.C. S.R.L. - Documentation Organization And Consultancy's top competitors are
Doc Pharma Official,
Stilmas,
Keyplants,
Fidia Pharma,
Mga - Masco Group Automation,
Fedegari,
Chiesi Group,
Masco Group,
Olsa,
Doppel Farmaceutici.
D.O.C. S.R.L. - Documentation Organization And Consultancy's categories are Pharmaceutical Manufacturing
D.O.C. S.R.L. - Documentation Organization And Consultancy's founding year is 1997
