Situated at Keshwana – Rajasthan 125km from New Delhi, the Manufacturing Facility is the State of the art factory for manufacturing the Pharmaceutical Formulations. This facility is capable of manufacturing Tablets, Capsules and External Preparations. The products belonging to wide range of therapeutic categories are being manufactured here.

This facility is designed to meet the highest standards of GMP in compliance with the US FDA and EU GMP requirements. The installed equipment and machinery are of international standard with high degree of automation. The clean rooms are spatially designed to meet the GMP requirement. The latest Quality Control instrument are available to maintain the highest quality control standards.

This unit proudly boasts to have delivered plethora of products (formulations) with unmatched quality. The very fact of having more than 500 product registration around the world under its belt, depicts the quality driven repute of the organisation. The brands, by virtue of their uniqueness have made a strong mark in their respective markets with a number of them being the brand leaders in their respective segments. The unit has been audited and duly approved by various regulatory authorities from South East Asia, Africa, CIS and South American countries


At SYNMEDIC LABORATORIES, Quality is our religion.

The Quality control Department is equipped with sophisticated instruments including U.V. Spectrophotometer, H.P.L.C, G.C. & F.T.I.R. Spectrophotometer for qualitative as well as quantitative analysis. Tests are performed by highly qualified, well trained and experienced analytical chemists for achieving the best in quality control. Accelerated and real time stability studies are carried out according to ICH (International Conference on Harmonization) guidelines to ensure that the quality of all products remains consistent throughout their shelf life. In-house facilities for Analytical Method Development and Validation as well as impurity profiling enable us to produce world class quality.

By virtue of its strong quality policy Synmedic Laboratories has been able to maintain its presence in the demanding export market for so many years.


The Regulatory affairs team in Synmedic Laboratories , has a high level of proficiency, and, it has played a key role in earning registrations of products across the globe. This sound technical backup gives further impetus to the business development activities.

The company has in-house capability to prepare Dossiers of the products as per CTD format, and various other requirements of different countries. Most of our formulations undergo clinical trials for Bio-Availability and Bio-Equivalence studies at reputed Clinical Research Organizations. Data from these studies is utilized to enhance the effectiveness of these formulations, which are part of our Dossiers.

The regulatory team at Synmedic has obtained more than a hundred registrations across the globe based on their proficient capabilities.


Strict adherence to cGPM norms is our motto. At Synmedic Laboratories, there is a continuous effort to improve the manufacturing systems and Standard Operating Procedures for better Quality Assurance.

The internal QA (Quality Assurance) Department ensures that the QMS (Quality Management Systems) are very well adhered too. The QA department ensures that any product before moving out of the manufacturing premises passes through stringent Quality standards. The staff in the factory is constantly exposed to various training programs so as to keep abreast with the new developments in the field of production and quality standards.

The company has maintained the WHO GMP status right throughout its operation in last more than 20 years. The company has received the approval from Phillipines FDA.


We at Synmedic endeavour to grow with a strong sense of responsibility. Our responsibility towards Society, Environment and Customers prevails without any scope of compromise. All our actions and deeds are earnestly carried out keeping their outcome and impact on the world around us.

The significant tenets of our approach include managing waste, controlling pollution, using energy efficient techniques thus we thrive to achieve equitable and accountable systems of governance and ensure environmental security.

Through our CSR activities, we introduce interventions that address critical needs and are sustainable over a period of time.

R & D

Research and Development department not just augments the on going technology driven manufacturing but also catapults the drudgery to newer heights. The R&D department contributes to the development of the process from Laboratory scale to the commercial scale development.

The challenges posed by stringent regulatory requirements in global arena are aptly annulled by the strong R&D. Our technical expertise efficiently amalgamates in sync with the most advanced testing equipment to attain optimisation.

R&D department of formulation unit primarily focuses on development of newer formulations with an objective to offer novel solutions with better patient compliance. To encompass the latest technological developments in the field of research, the technical team is well equipped with most up-to-date equipment