Knors Pharma has been exceptionally meticulous with the work done, to make sure it is of the best quality.
Our team consists of highly skilled and experienced individuals who have been working with the company for years now.
Having the versatility of experiences we provide efficient and integrated solutions for your company to comply with regulatory requirements.
Led by our director our experts make sure the team focuses on the quality of service to compliment the business.
We at KNORS Pharma Solutions LLP are a team of qualified and experienced pharma professionals working to provide solutions to the pharmaceutical industry.
KNORS Pharma performs third party evaluation (Gap Analysis) of pharmaceutical manufacturer through its professionally designed tool for compliance level assessment. We help the pharma companies to implement comprehensive CAPA and prepare them for inspections from regulatory agencies like USFDA, MHRA, MFDS, EDQM. Our GMP auditors are qualified by international bodies like Intertek, France and Forum Auditorias, Spain.
KNORS Pharma experts are professional trainers on cGMP and Pharmaceutical Quality Management Systems.
KNORS provides support to the pharma industry in setting up new project with technology development, Technology optimization and technology transfers through validations.
We Design, Rationalize and Integrate QMS also Minimizes the losses in manufacturing by increasing the efficiency, reducing the rejections.
Experts in KNORS Pharma Solutions are qualified trainers on cGMP and Pharmaceutical Quality Management Systems. KNORS conducts trainings and workshops on current focus areas of regulators such as Data Integrity, OOS Root Cause analysis and CAPA, Quality Matrices, QbD, Handling of regulatory audits and Certification of internal Auditors
KNORS Pharma provides services in Drug Regulatory Affairs. Our regulatory experts compile the dossiers (DMF, ASMF, APIMF, CESP and ANDAs), publish in eCTD format through software and facilitate to file in regulatory agencies. Experts help the companies in addressing the deficiencies of regulatory agencies if requested during review of application.
IRCA Certified Auditor and QMS/cGMP Expert
Expert in Qualification/ Validation, Technology development, optimization, transfer
QMS Expert and Qualified Auditor
Manager - contract manufacturing site development and material management
Qualified Trainer and GMP Consultant- Expert in Quality Systems of OSD, Sterile and Injectables
Microbiologist and Audits Coordinator