Quality Control

Dishman has a long history of applying quality assurance and good manufacturing practices in development, production and quality control process. The company undergoes stringent quality control for all stages of manufacture and delivery. DISHMAN applies the total quality management approach using ISO 9001:2000 methodology and cGMP.

Quality control laboratories are well equipped with the latest instrumentation like Spectrophotometers, GLC, HPLC. Quality up-gradation of our products is a regular developmental feature of DISHMAN´s Q.C. Department, resulting into achieving products of highest international standards.

Analytical Development Laboratory:

DISHMAN has first hand expertise in the development of analytical methods; validation of analytical test procedures; isolation & characterization of new molecules including impurities, particle size analysis and much more.

Quality Assurance:

DISHMAN´s QA department is instrumental in the preparation of protocols and monitoring qualifications, strict process control; process validations; stability studies; training & development; self- inspection & audits; systems and procedures and relevant documentation. In addition to these routine responsibilities, our QA department also performs following functions related to contract research & manufacturing operations:

• Preparation of various SOPs related to production, testing, release, packaging & labeling of the APIs.
• Preparation & approval of various IQ & OQ protocols.
• Execution of IQ/OQ & PQ in co-ordination with the technology department and equipment supplier & preparing IQ/OQ reports.
• Preparation & approval of various validation protocols like process validation protocol, rework & milling validation protocols.
• Preparation & approval of stability protocols, cleaning records & batch records.
• Preparation of validation reports, stability reports of starting materials & actives.