Services
Accredited Reference Laboratory
An accredited laboratory is one that undergoes regular evaluation and approval of its performance by a supervising authority, such as the Food and Drug Administration (FDA), in accordance with the requirements outlined in quality standards based on international standards. Through these evaluations and assurance of adherence to Good Laboratory Practices (GLP) across all functional areas and documentation, the test results conducted by the accredited laboratory are recognized and approved by the FDA.
Research Services
**Our Core Strength: Research and Development**
Our primary strength lies in our R&D unit, which excels in developing complex generic and technologically advanced products through specialized formulation and analytical teams. Our scientists collaborate with the business development team to generate innovative ideas and capitalize on market needs. Formulations are designed based on **Quality by Design (QbD)** principles to introduce robust, regulatory-compliant products to the market.
As a generic pharmaceutical company, we specialize in developing complex technology formulations and niche products, including **immediate-release, modified-release, and nano-based formulations**. Over the years, we have acquired expertise in conducting pharmacokinetic studies and bioequivalence trials, enabling us to launch medications in international markets.
Our contract R&D services encompass **formulation development, product development, and technology transfer**. By defining the Target Product Profile (TPP) and adopting a systematic and efficient approach, we deliver high-quality products ready for commercialization. Our research capabilities have not only proven to be profitable but have also earned us a distinguished reputation for quality and expertise.
Manufacturing Services
We provide the best infrastructure and methodologies for the production of active pharmaceutical ingredients (APIs), semi-finished products (pellets and DC), and oral liquids (syrups) with the highest standards of quality, compliance, transparency, safety, environmental policies, and ethics. Manufacturing at our organization is GMP-compliant and always considers HSE (Health, Safety, and Environment) principles to deliver top-notch healthcare manufacturing services.
Our state-of-the-art production lines are equipped with advanced machinery and various capacities, allowing for continuous monitoring and control of operations to meet the growing regulatory and market demands. We adopt the best industrial manufacturing practices across all operations to ensure the highest product quality standards.
In manufacturing, the principle of "quality"—defined as a benchmark of excellence or a state free from defects, deficiencies, and variations—is guaranteed through strict and consistent adherence to measurable standards. This ensures uniformity in output, meeting the specific needs of our valued customers.
With 20 production lines and an annual capacity of 5,000 tons of pharmaceutical APIs, we are ready to welcome partnerships for joint collaborations and contract manufacturing in the pharmaceutical industry.
Equipment Capabilities of TAMAD Accredited Laboratory
The TAMAD Accredited Laboratory, in line with other advanced laboratories, is equipped with state-of-the-art instruments, including HPLC, GC, UV, TOC, IR, Dissolution Test Apparatus, Melting Point Determination Device, Viscometer, Centrifuge, Karl Fischer Titrator, Potentiometer, various Incubators, Furnace, Sieve Shaker, and all necessary microbiological laboratory equipment such as Ovens, Autoclaves, and various Laboratory Hoods, all sourced from the best European and American brands.
The laboratory has the capability to perform all physicochemical tests, instrumental analysis, and microbiological (non-sterile) tests in accordance with reputable pharmacopoeias (such as BP, USP, etc.) or internal analysis methods (In-house).
Main factory address
Tehran, 28th kilometer of the Karaj Special Road, opposite Atmosfer Metro Station, Drug Materials Production Company (Temad).
email: info@temad.com
The vision of Temad Company by 2027
To become a knowledge-based, efficient, export-oriented, and leading company in the production of high-quality active pharmaceutical ingredients and semi-finished pharmaceutical products in West Asia.