Research & Developmnet

Research and Development is the cornerstone of Taseer’s mission. Taseer has built considerable R & D Department. Taseer has built up considerable R & D strength. centered around a knowledge–base of a pharmacist , chemist and a manager who heads R & D department.Our major strengths lie in the development and commercialization of generic active pharmaceutical ingredients and dosage forms, in line with international regulatory and quality requirements. Innovation is our strategic and tactical priority and we agree with Tom Peters “Get innovative or get dead,” so we believe in self sustaining and long lasting innovative effect. Scope of R & D Department covers following activities, which are focused on product’s efficacy, safety, stability and economy. The activities are as follows:To design and develop new products.To improve current formulations keeping in view Quality with economy.To study the market and in house complaints relating products and make proper remedies for them.To conduct stability studies of the trial batches and first three commercial batches of new product as a trial and design validation and having an appropriate data.To check the stability of near to expiry /expired products received from market or in-house retained samples of Post Market Studies. Extension in shelf life of the products based on proper stability data.To establish and implement the validation system on processes, methods and personnel.

Quality Control

The QC department comprises of highly skilled and experienced professionals using sophisticated testing procedures for the testing of active pharmaceutical ingredients, recipients, packaging components and finished pharmaceutical dosage forms are carried out as per latest pharmacopoeia standards. We have the evaluation and approval system for different suppliers at our Quality Control Laboratory.

Retaining Samples of Finished products

Other than Routine testing, QC also has samples retaining room (for legal reference).Samples from each batch are kept over there for legal reference and as a record for stability studies which is being carried out according to the written standard procedures. The samples of finished items are retained up to one year after expiry as of the ministry of health to ensure the shelf life of the product. Retaining samples are very much helpful to any investigator against the product complaint.

Calibration Program

Calibration is a set of operations that establish, under specified conditions the relationship between values of quantities indicated by a measuring instrument (or values represented by a material measure) and the corresponding values realized by standards. Here in global pharmaceuticals, we have a periodic Calibration program for all the equipments/instruments. Calibration are being done internally and some times through external parties along with traceability as per standards.

Microbiology laboratory

Microbiology laboratory is the vital part of pharmaceutical industry in the modern era. Testing of sterile as well as Non-sterile dosage forms as per standard procedures is inevitable so that contamination free products to be supplied to the end user. In Taseer Herbal Laboratoreies, we have well furnished micro laboratory with highly skilled professionals duly equipped with state of the art instruments for the various microbiological testing of sterile products, Area monitoring, water testing  for Pyrogen testing.Sterility testing of the finished products is performed to ensure the sterility of the parenteral products prior to their delivery to the market.

Quality Assurance

We have a strong set up of Quality Assurance to ensure the in built quality of the products. Highly skilled, experienced and professional staff, not only ensures the strict compliance of Local drug rules. Quality Assurance is a fully independent department directly reportable to the chief executive and it comprises QA Manager, Asst. QA Manager. and QA Officers . It has professionally competent and experienced officers specifically having their duties for various sections like separate staff for oral products and separate staff for sterile production for monitoring and inspection of processes.

Quality Assurance has the following objectives:

To assure high quality production by in process sampling, inspection and testing throughout the process.
To assure and maintain consistent quality production by in process sampling, inspection and testing throughout the process.
To ensure that the products are meeting all the required standards /specifications during all the manufacturing and packing processes.
To monitor and provide guidance to the stakeholder regarding storage of products so that the product may not loose its efficacy and potency due to environmental factors i.e. temperature, humidity.
To conduct training of all quality assurance staff to achieve quality objectives.
To conduct a post marketing surveillance by assigning duties to medical representatives to send samples of their respective areas.