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Compliance Consultation & Validation Services
Tofflon provides consulting services and validation services for all types of pharmaceutical companies to meet the current GMP compliance in accordance with NMPA, EU, US, PIC/S, WHO and other relevant GMP compliance services, including one-stop services from URS, GMP compliance audit of engineering drawings, design audit, PQS system setup, EPC validation management and validation execution, training, auditing, and GMP certification consulting, etc. Tofflon can help companies to achieve and maintain GMP compliance throughout the product lifecycle and improve your operational performance and reliability. We look forward to working with you to create a better future!
Advanced Production Base
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(M+E+C)&AI&
Relying on the understanding of regulations and processes, provide reliable end-to-end equipment and facilities from R&D to commercialization; Through planning and design, procurement management, engineering construction, system verification and other processes, integrated delivery of factories with specific functions; Provide core process consumables such as culture medium, resin, filter and single use reaction bag to assist process optimization and solve the problem of stock solution production; Relying on the time experience of informationization and intelligence, we will provide forward-looking and professional digital intelligence planning to help enterprises transform digitally.
Address:
No.1509 Duhui Road,Shanghai,China,201108
Sales: info@tofflon.com | Service: service@tofflon.com
Copyright © 2020-2021 Tofflon Science and Technology Group Co., Ltd. All Rights Reserved. Shanghai ICP No.13216461 -1
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