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We have the necessary wherewithal to provide all the services that are required to maintain a pharmaceutical industry in a perpetually compliant state by providing all the services that are required such as:
Auditing & Compliance Monagement Project Management Formulation Development Qualification & Validations Drafting & Writing of Documents Training Regulatory Affairs & Preparation / Review of Dossiers Operational Excellence Education It has team of experts and promoted by a Mr. T.Ramarao is an M.Pharm (Pharmaceutical Technology )-in the year 1985 , from Department of Pharmaceutical Sciences, Andhra University, Visakhapatnam, India. He was awarded G.P.Nair Gold Medal by Indian Drug Manufacturers Association (IDMA) ,Mumbai & Nageswara Rao Pantulu Gold Medal by Andhra University for standing first In B.Pharm ,1983. He has over a period of 30 years of experience, having worked in medium and large scale organizations like Ranbaxy, Hoechst Marion Roussel Ltd, Biological E Ltd, Procter & Gamble Hygiene and Health Care Ltd ( operated by SRL) etc. He has discharged at executive as well as leadership responsibilities in the areas of design & development, manufacturing, qualification & validation, manufacturing, operations management, quality assurance, quality management, audits & compliance, regulatory affairs, technology transfer, project management, development of formulations and operational excellence .He led team of experts in preparing the regulatory filings, facing GMP inspections / audits and responding to the inspectional observations of various regulatory agencies, such as WHO, ISO, USFDA, UK-MHRA, etc A few reasons to partener with us: a) You get all services with regards to GMP requirements for US FDA, UK MHRA, TGA, WHO GMP, ISO 9000 etc., at Sai Pharma Consultants under one roof.b) Committment to our Clients c) Committment to Quality & delivery,Experience in Industry,d)Committment to economic & sustainable design.. Commitment to Our ClientsCommitment to Our Clients Commitment to Our Clients + Read More
Auditing & Compliance Monagement Project Management Formulation Development Qualification & Validations Drafting & Writing of Documents Training Regulatory Affairs & Preparation / Review of Dossiers Operational Excellence Education It has team of experts and promoted by a Mr. T.Ramarao is an M.Pharm (Pharmaceutical Technology )-in the year 1985 , from Department of Pharmaceutical Sciences, Andhra University, Visakhapatnam, India. He was awarded G.P.Nair Gold Medal by Indian Drug Manufacturers Association (IDMA) ,Mumbai & Nageswara Rao Pantulu Gold Medal by Andhra University for standing first In B.Pharm ,1983. He has over a period of 30 years of experience, having worked in medium and large scale organizations like Ranbaxy, Hoechst Marion Roussel Ltd, Biological E Ltd, Procter & Gamble Hygiene and Health Care Ltd ( operated by SRL) etc. He has discharged at executive as well as leadership responsibilities in the areas of design & development, manufacturing, qualification & validation, manufacturing, operations management, quality assurance, quality management, audits & compliance, regulatory affairs, technology transfer, project management, development of formulations and operational excellence .He led team of experts in preparing the regulatory filings, facing GMP inspections / audits and responding to the inspectional observations of various regulatory agencies, such as WHO, ISO, USFDA, UK-MHRA, etc A few reasons to partener with us: a) You get all services with regards to GMP requirements for US FDA, UK MHRA, TGA, WHO GMP, ISO 9000 etc., at Sai Pharma Consultants under one roof.b) Committment to our Clients c) Committment to Quality & delivery,Experience in Industry,d)Committment to economic & sustainable design.. Commitment to Our ClientsCommitment to Our Clients Commitment to Our Clients + Read More
Nature of Business
ConsultantsTotal Number of Employees
Upto 10 PeopleYear of Establishment
2015Legal Status of Firm
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