Regulatory

Systochem laboratories is a WHO GMP certified company and has ISO 9001:2008 certification

Systochem laboratories is situated in an approved industrial area known as Roop Nagar industrial area, Loni , Ghaziabad , located on the periphery of Delhi. The location is ideal and hygienic approached to the main highway and in the pollution free environment. The factory premises is away from open sewage, drains and from other factories which produces disagreeable odour, fumes, large quantity of soot, dust and smoke.

In keeping with the needs of the time, the venture is totally eco and environment friendly. The manufacturing process is being disposed off as per the industrial norms and guidelines. Strict compliance to the rules and regulations set forth by the pollution control board are being adhered to. Systochem laboratories looks for the stronger support of its people to adhere to cGMP requirements. Systochem laboratories is continuously upgrading its facility not only in quality but also its management & administration control.

Quality control
The lifeline of the company and strength to recon with, we believe that "He who has the most stringent quality control will have the best product". The company has a self-s ufficient laboratory in place and have some most dedicated personnel's who are highly motivated to lead this organization. Apart from the Pharmacopoeia requirements the laboratory is equipped to conduct various tests that are required to make a quality product. Capability to identify the impurities and to study the degradation of the products helps to improve the product quality and improves the general understanding of the products.

Quality Assurance
Systochem Laboratories has ever since strived to improve its existing facility by carrying out regular inspection and updating of technology for its products and processes and thus adhere to cGMP. To ensure that the cGMP standards are met and products comply with international quality standards, quality control measures having been imbibed at various stages of productions-from approval of raw materials to goods in-process as well as monitoring of the manufacturing process and extends up-to checking of finished goods. Quality assurance in the production is adhered by strict in-process controls and by validation and optimization of the process to improve quality and production.

CAPA: Corrective and Preventive actions
The company has in place a complete written program under CAPA and the procedure is well defined
Systochem Laboratories under CAPA is analyzing processes, work operations, quality audit reports, quality records, service records complaints, returned product and other sources of quality data to identify existing and potential causes of nonconforming product and other quality problems. Appropriate statistical methodology is employed where necessary to detect recurring quality problems.