Fides Biocare Kathodara, Surat, Gujarat

FIDES BIOCARE.are Manufacturer, Supplier and Exporter of variegated Pharma products that consists of Finished Products, OTC products, Nutraceutical Medicines.
• We are evolved as a trailblazer in Pharmaceutical industry, operated office at Pharma hubSurat in (Gujarat), India.
We envisage being provider of quality products across the globe in Human &VeterinaryPharmaceutical products.
• We promise better healthcare and longer life for every human being at very affordable prices. Fides Group Inc.is dedicated to development, manufacturing and marketing of quality Pharmaceutical to meet growing demand of healthcare.
• We cater to the demands of the Asia Pacific, Latin America, Middle-East, Africa, CIS country, Asia Pacific etc. by understanding their requirements and accordingly developing pharmaceutical drugs as we do under contractual manufacturing.
• We have the flexibility to meet your needs under strict quality guidelines.
• We approach our business seriously and provide value and quality to our customers every day. Fides Bioexport devotes extensive effort in providing medicines to third world countries. Tablets Lotion
Oral Liquid Eye / Ear Drops
Dry Powder Toothgel
syrup Mouthwash
Capsules Irrigation solutions
Softgel Capsules Small volume parenterals
Injectables Large volume parentrals
Ointments Reconstituted powders
Cream
Anti-infective Hormonals
Antituberculosis Anti-Asthmatics/Cough and Cold and Nasal Sprays
Oncological Products Gaestro-intestinal Products
Antimalarial cardiovascular/Lipid lowering Agents
Psychotropic and Antidepressants Bone modulating Products
Analgesic Urological and Erectile dysfunction Products
Dermatological Products Heamatonics and Nutritional supplements
Anti-diabetic Gynecological Products
Appetite Stimulant Veterinary medicines
Diabetic and Endocrine Products other
• Preparation of Dossier files As per country specific guidelines
• Review of dossier file As per the Regulatory Authority’s guidelines
• Assistance in MOH schedule for product life cycle management
• Filing of Registration dossiers for submission to various regulatory agencies all over the world (including CTD format & ACTD Format).
• Non-clinical and clinical overviews and summary writing through literature search from published studies / registered studies and research articles having good impact factor.
• Drafting the MRA query during the registration procedures and responding to the same
• Post approval Changes or reregistration for product life cycle management by assisting the clients for additional data generation
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