Move into the industry with confidence. Knors Pharma is a leading regulatory and scientific consulting firm.
Working with businesses of all sizes, Knors Pharma has helped obtain over 150 Knors Pharma licences for federal commercial production, research, testing, and retail. Growing a new business?
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Know About Knors Pharma
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, Eurofins, PQE, and Forum Auditorias. 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 technology transfers through validations and QMS design.
Our mission and values
Our mission is to provide highly professional services to the pharmaceutical industry and become the most trusted pharmaceutical consultancy company in world.
Our values are:
Services We Offered
KNORS Pharma qualified auditors perform third party audits of manufacturers of Drug Products, Active Pharmaceutical Ingredients, Raw Materials(KSM), Packing Materials, Drug Intermediates, excipients and testing laboratories. Our technical experts are IRCA certified QMS lead auditors and trained to perform audits as per international standards.
Our experts perform third party evaluation and gap analysis with a quantified tool to assess the company’s state of regulatory compliance. We help the companies in designing CAPA for deficiencies raised by regulatory agencies(inspections).
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.
We at KNORS have come up with new vertical of developing the source of pharmaceutical materials (Drug Products, APIs, Intermediates and starting materials). Our team of business development along with regulatory experts develops the manufacturing sites for clients of regulatory markets; USA and Europe.
Consultancy Services | GMP Audit Pharmaceutical | GMP Gap Analysis Audit | GMP Training | DMF/Dossier Preparation | cGMP Consulting Services | Quality Management Systems | Technical Document Writing
Our movements keep various platforms of due diligence such as science and technology, intellectual property, clinical development, and regulatory due diligence reports for majorly pharmaceutical industries and development.
PHARMACEUTICAL & MEDICAL
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, O, OS Root Cause analysis and CAPA, Quality Matrices, QbD, Handling of regulatory audits and Certification of internal Auditors.KNORS Pharma qualified auditors perform third party audits of manufacturers of Drug Products, Active Pharmaceutical Ingredients, Raw Materials, Packing Materials, Intermediates medical devices and biotechnological products. Our auditors are trained to perform audits as per standards.