For all manufacturing processes, taking place in Daffohils Laboratory Pvt. Ltd. we have teamed up with some of the best manufacturing units that are certified by WHO - GMP, GLP & ISO. In addition to producing tablets, capsules, syrups, and injectables in the beta-lactam and non-beta-lactam range, we provide multi-disciplinary pharmaceutical manufacturing services. Our company produces herbal products, ointments, and other liquid formulations as well.
We pride ourselves on the high quality of our products that are a result of the world-class infrastructure, equipment, tools, and operations in our manufacturing units. We can select the best
packaging for a product based on the requirements to ensure its protection throughout its shelf life from a wide range of packaging options. The raw material is purchased in accordance with all specifications and the finished product is also dispatched in accordance with the specifications.
Quality Control (QC) and Quality Assurance (QA):
Our manufacturing operations are regularly monitored by various regulatory agencies and third parties. By doing this, we can ensure that our manufacturing practices comply with internationally recognized best practices. For our business partners, healthcare providers, and final consumers, our assurance becomes the foundation and the trust.
As part of our quality assurance & quality control department, we ensure all good manufacturing practices (cGMP) are followed when developing, manufacturing, packaging, storing and dispatching formulations.
From raw material procurement to formulation dispatch, Standard Operating Procedures (SOPs) have been drafted for every process. All steps of the production process are subject to quality control. In addition, Good Laboratory Practices (GLP) guidelines are also followed for the ingredients and formulation.
All these requirements are met by our partner companies through:
- SOPs and cGMPs are regularly audited in manufacturing, laboratory, and other areas to ensure compliance. Audits are conducted by third parties to ensure that quality is not compromised. Facility audits, equipment audits, and system audits are also conducted to ensure calibrations and other malfunctions are not revealed.
- Reviewing SOPs periodically improves the efficiency and productivity of each procedure. Additionally, protocols and reports are periodically reviewed for the qualification & validation of processes, as well as standard operating procedures, manufacturing methodology, and analytical methodology.
- Tests performed during the production process at every stage are called In-process Quality Control (IPQC). These tests are performed to reduce errors. And whenever any mistake is detected, corrective and necessary measures are adopted at the same time so that the final product is composed as expected.