Please visit us Vietnam Medi-Pharma Expo, stall C160, August 1st- 3rd SECC Ho Chi Minh City, Vietnam. Please visit us @ CPHI Middle East & Africa, stall H72, September 16th – 18th ADNEC, Abu Dhabi, UAE.

ABOUT US

SAINOR LABORATORIES PRIVATE LIMITED, UNIT - II PHARMA DIVISION is located at Jeedimetla, Hyderabad, India (Formerly known as Sainor Pharma PVT. LTD) established in the year 2006. We manufacture Delayed Release Pellets, Extended Release Pellets, Modified Release Pellets & Sustained Release Pellets of various strengths practicing cGMP standards. We provide pellets of highest quality standards to our customer’s satisfaction.

QUALITY ZONE

Quality Zone Consists of Quality Assurance and Quality Control.

Our quality systems are designed in line with Schedule M, ICH and ISO 9001-2015 Standards.

The organization maintains the highest standards of quality for all products by following current Good Manufacturing Practices at each and every stage of manufacturing.

Deliver the products that consistently meet the expectations of the market and customer requirement.

In Quality Control day to day analysis like Raw and Packing Materials, In-process, Finished Products and Stability samples along with Analytical Method Validations by using sophisticated analytical instruments.

QUALITY SYSTEMS

  • Training
  • Change control
  • Compliants
  • Corrective action & Preventive action (CAPA)
  • Deviation
  • Return Goods/ Recall
  • Risk Assessment
  • Out of Specifications (OOS)
  • Internal Audits
  • Vendor Qualifications
  • Good Documentation Practices
  • Investigations

R & D

PROCESS R&D

The Process Development Centre work on development of process and scale up from gram scale to pilot scale. The process optimization, pilot studies, pre-validation batches, validation of process and transfer of technology to plant.

ANALYTICAL R&D

Sainor Laboratories Private Limited, uses State-of-the-Art-facilities to develop analytical methods for evaluating quality of raw materials and final products. Facility is capable to analyse the impurity profiles and identify degradation of their active substances with the use of sophisticated instruments such as HPLC and GC.

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