Newlystar (Ningbo) Medtech Co.,Ltd.

Company Profile
Newlystar (Ningbo) Medtech Co.,Ltd.

Newlystar-Medtech is a well established and professional supplier of Finished Pharmaceutical, Active Pharmaceutical Ingredient(API) and Medical Devices. With a proven track record of passed years, Newlystar-Medtech has been recognized by her customers as a high-quality and reliable supplier not only on products, but also on assistance for audit and improvement of GMP level, quality management system, EHS management system and registration dossier support, etc.

The essence of Newlystar-Medtech's activites, is a commitment to her customers with professional service and high-quality products with effective cost and innovative solutions. All pharmacists work in Newlystar-Medtech like a bridge link the customers and Chinese manufacturers, especially, their professional working is to make the formulation manufacturers who is familiar with Chinese Pharmacopoeia to understand well the international requirement, to ensure the success of customers.

The advantages on professional working and strongly representative base on first-class manufacturing partners in China, enable Newlystar-Medtech to provide her customers with a wide range and high-tech products, best services and capabilities for their actions in tender, distributing and improvement in their national healthcare system. Newlystar-Medtech also dedicates herself to sourcing quality medical products for Chinese market.


Services and capabilities include:
1. Sourcing quality manufacturer
2. Contract manufacturing;
3. Conduct audits to suppliers (pharmaceutical plants);
4. Consultation on audit and improvement of GMP level, quality management system and EHS management system;
5. Regulatory support, registration dossier working;

 

Newlystar Medtech, your professional one-stop China Souring Partner.

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Year of Establishment: 20

Total Assets(USD): 20,000,000 To 24,999,999

Total Number of Staff: 20 to 29

Main Competitive Advantages:

Other Competitive Advantages: 1. Rich experiences in passing international GMP auditing. Include but not limited to EMEA, US FDA, TGA, INVIMA, PIC/S, Germany, Peru etc. 2. Rich experiences in registration/dossier support. CTD format. 3. Big business with China manufactures whose management on GMP is good. We classify our suppliers with GMP management level and product quality level, not by their turnover. Even there are correlation between them to some extend.

Patents and Copyrights:

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