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pharmaceutical consultancy services
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Saheb Pharmaceuticals LLP and healthcare specialists serve customers in the pharmaceutical, biotechnology, and medical device industries at all phases of product development in Pune, Maharashtra. Our team of scientists and regulatory affairs professionals has extensive expertise in nonclinical safety testing, manufacturing, submission preparation, regulatory agency contacts, risk/safety assessments, medical writing, and other areas. We endeavour to create strategies and provide solutions that satisfy our clients with pharmaceutical consultancy services. We built our firm to make regulatory compliance easier and faster. Our work culture distinguishes us as distinctive, valued, and distinct. We wholeheartedly support the regulated professions and their practitioners. We are dedicated to offering intelligent regulatory technologies and assisting regulatory professionals in their pursuit of excellence.
Clinical Research Service
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Afra pharma consultant offer to conduct, manage and monitor multicentre clinical trials in a wide range of therapeutic areas and monitor be studies in india and abroad. We have a special interest in independent clinical trial monitoring work in india and abroad for sponsors from india and abroad. medical writing & clinical studies bioavailability bioequivalence clinical trial studies analytical solutions reports on bio availability / bio equivalence studies clinical trials studies prepare periodic safety update report (psur) preclinical studies like toxicity, carcinogenicity, and teratology & reproduction toxicity biosciences services: we are in association with iso certified, ichgcp compliant clinical research & consulting firm which is dedicated to provide clinical study related services for pharmaceutical and biotechnology product development sculpted to offer high quality design, conduct and analysis of a clinical trial which constantly try to innovate in order to provide easy solutions to our clients for their prestigious projects. To accomplish this, we strive to provide our clients with exceptional services under one roof for the vast sector of clinical trial management and bioinformatics developments. In clinical research, our services range from site services to sponsor related, regulation of monitoring issues, management of the clinical trial data, precise scientific writing and the developing post marketing strategies; strictly adhering to the respected regulatory compliance summed up with our personal commitment to time management and unbiased report submissions.
Looking for Bioanalytical Services Providers
Pharma regulatory Affairs services
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We offer- • Quality System Certification & Documentation: Preparation, Maintenance, guidance for FDA, WHO-GMP, USFDA, MHRA, EDQM • Validation & Qualification: Area, Process equipment, process, water system, HVAC, Cleaning, Personnel, Analytical services, Lab instruments • Internal Audits & Customer Audits • cGMP audits • Vendor audits & Vendor qualification • Laboratory set up, up-gradation to FDA, WHO- GMP, USFDA, MHRA, EDQM, GLP & GMP Standards. • Recruitment and Training • Specifications: Raw material, Packing material, In Process materials & Finished products specification • Ayurvedic formulation development & documentation as per FDA requirements • ISO 9001:2000 & PS 9001:2000, Regulatory assignments.
Pharma Warehouse
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Pharma Warehouse, Thermal insulation foam, Reflective Insulation
psychological tests
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psychological tests, entrepreneurship development program
