Parume Bio-Services Inc. was established in 2022 in Suzhou, P.R. China. The company mainly provides professional pharmaceutical engineering solutions and related professional services to domestic and foreign pharmaceutical enterprises, clinical services, and pharmaceutical contract manufacturing organizations (CMOs).
With a diverse background in pharmaceutical engineering, we can provide pharmaceutical companies with conceptual design layout of facilities, specific design and estimation of equipment and facilities, and risk-based confirmation and verification services. The company can advise clients on these areas.
When you are planning for a new manufacturing facility, upgrade of process equipment or expansion, it all starts with the process design.Understanding the process and being able to translate it into a cGMP compliant facility design is key.
We have developed an extended V-model.This V-model offers seamless integration of Quality by Design as defined by ICH Q8 and a modern risk-based approach as defined in ICH Q9 and GAMP 5 Risk-Based Approach to Compliant GxP Computerized Systems.
Parume is offering consultant services to manage your commissioning, qualification, validation and Quality Management System (QMS) projects for all types of pharmaceutical and Clinical trial facilities and system.We also provide Quality Manuals, including management and supporting SOPs.
Starting up a new manufacturing building often requires training of operators and maintenance personnel. Parume can provide tailor-made training programs for your new facility covering areas such as:
Hands-on training on process and utility equipment.
Maintenance training
How to work in a GMP facility
Parume continues to serve you even after your project is installed and in operation. We can be your partner when it comes to keeping your facility and equipment in good working order and your production running smoothly. Should you require technical assistance.
On-site service
Service contracts
Documentation Training
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