


Bellatriks Project Management, GxP & Validation Partner Revenue
Pharmaceutical Manufacturing • Denmark • 1-10 Employees
Bellatriks Project Management, GxP & Validation Partner revenue & valuation
| Annual revenue | $256,665 |
| Revenue per employee | $86,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Pharmaceutical Manufacturing industry and current estimated revenues | $821,328 |
| Total funding | No funding |
Key Contact at Bellatriks Project Management, GxP & Validation Partner
Kim Lauritzen
Member of the Board of Directors
Company overview
| Headquarters | Denmark |
| Phone number | +4553838475 |
| Website | |
| NAICS | 3254 |
| SIC | 283 |
| Keywords | Project Management, Quality Assurance, Validation, Qualification |
| Founded | 2016 |
| Employees | 1-10 |
About Bellatriks Project Management, GxP & Validation Partner
Bellatriks is an independent consultant company that offers Project Management and GxP services e.g. GMP, GDP and Validation to Quality Assurance and Manufacturing organisation in pharmaceutical and Medical Devices companies. We have many years of experience gathered in Consulting Engineers e.g. NNE Pharmaplan, Niras and renowned Pharmaceutical and Medical Device companies, e.g. Novo Nordisk A/S, Lundbeck A/S, Codan Medical ApS. Industries: Aseptic / Sterile manufacture Biotechnological production API production Medical Devices Combination Products We can support you e.g. by: Fast track project management, revamps of plants within the pharmaceutical and confectionary area in close cooperation with manufacturing and R&D. Turn key project management within the pharmaceutical industry. Facilitating project workshops and design reviews to ensure that all requirements are met for all stakeholders. Prepare for an FDA or EU GMP Inspection, perform Internal Audit. Perform Supplier Audit or Quality Assessment at CMO on behaft of the client. Support your QA organisation with QP/QA tasks regarding review of Batch Record, APR/PQR Perform validation tasks in Cleaning / Sterilization / Transport processes. Perform Computer Systems Validation acc. to GAMP 5, FDA 21 CFR Part 11 and EU GMP Vol. IV Annex 11. Writing Validation Master Plan, Validation Master Plan Report, Validation Plan, Validation Plan Report etc. Writing SOP's, Non Conformities (deviations), Incl. Root Cause Analysis Mapping Temperature of warehouses and cold rooms. Giving on-site GMP, GDP and Validation Training/Workshop to the Pharmaceutical, Medical Device.
Employees by Management Level
Total employees: 1-10
Seniority
Employees
Funding Data
Bellatriks Project Management, GxP & Validation Partner has never raised funding before.
Bellatriks Project Management, GxP & Validation Partner Tech Stack
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