Experience

Guerison Pharmaceuticals Inc

• United States
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Director Global Business Development

  • Jan 2017 - Present

  Guerison Pharmaceuticals Inc offers a complete solution to manufacturers, distributors, and procurement companies within the field of Pharmaceuticals and Clinical Research Industries Established in 2015, we are a global, pharmaceutical wholesaler with customers ranging from private practices, clinics, hospitals, research institutions, international importers and pharmacies worldwide. We carry over 30,000 FDA approved pharmaceuticals and health products as well as medical supplies. All of our products are currently for sale in the USA and approved by the FDA. Guerison Pharmaceuticals Inc is your partner for future medicine Global Comparator / RLD/ Innovator Products Sourcing USA, UK, EUROPE, CANADA, FRANCE, BRAZIL, JAPAN AND AUSTRALIA BUY BACK-RLD EXPIRY FROM USA · Single Batch Procure with long/Short expiry · Data logger, Controlled Shipment · Narcotic/Psychotropic RLD · REMS Products · As per drug return good policy in USA--We have Reverse distribution License for RLD Expiry Product or Near to expiry product from USA · You will get 10 to 60 % return money or credit note from our end (3 months’ timeline in terms of a credit note ). · Product is near to expiry product from USA and after expiry 6 month only. Show less



TECHLIGAMENT LIFE CARE GROUP

• India
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Director at Pharmaceutical/Clinical Research Organization

  • May 2011 - Sep 2022

  Techligament is specialized Pharmaceutical, Clinical Research and Healthcare Industry Consulting firms. Having office in Mumbai, Maharashtra, Mumbai We dealing with major Pharma companies in all areas like –Clinical Research, Formulations Research, Chemical Research, Analytical Development, Pharmacology /Pharma Biology, Regulatory Affairs, Quality Assurance / Technical, Production, Sales & Marketing, Medical Services, etc. Where we coordinate and conduct following Services: ( For Local and Non/Semi/Regulated Market) 1. REFERENCE PRODUCT SUPPLY: 2. CLINICAL TRIALS 3. PRE-CLINICAL TRIAL 4. BIO-AVAILABILITY AND BIO-EQUIVALENCE 5. ANALYTICAL SERVICES 6. SUPPLY AND SUPPORT 7. REGULATORY SUPPORTS 8. MEDICAL WRITING WORK 9. CONTRACT RESEARCH MANUFACTURING 10. BUSINESS OUTSOURCING 11. PLACEMENT/RECRUITMENT SERVICES 12. SCIENTIFIC LITERATURE 13. FINISHED/API/RAW MATERIAL/CHEMICAL PRODUCT SUPPLY I look forward to a mutually beneficial business relationship ahead. Regards, Mr.Lalit Wani Techligament ( Unit of Naukricare) Kalyan (W), Thane 421301 Maharashtra, India Mob No/WhatssApp: +91-9167920553/9967596296 Skype: techligament and naukricare Email: techligament@gmail.com or pharma.clinicalcareer@gmail.com Website: http://www.techligament.com or http://www.naukricare.in Show less



Tata Consultancy Services

• India
• IT Services and IT Consulting
• 700 & Above Employee

• Drug Safety Specialist (Pharmacovigilance Division)

  • Jan 2009 - May 2010

  Processing and reporting of AE/SAEs reports. (Clinical and Spontaneous cases) Gathering relevant information from source documents and entering in safety database (Advent / Sapphire). Analyzing and evaluating individual cases and collecting, collating and reporting adverse event data and drafting narrative for each case. Coding of Adverse Events, patient history, product indication, suspect and concomitant drugs using Medical dictionaries (eg. MedDRA). Conducting internal QC, maintaining various project trackers for entire team and reporting to Team Leader. Preparation of Periodic Safety Update Report (PSUR), providing medical evaluation comments (CCC) and submission to regulatory authorities as per timeline. Show less



Bioequivalence CRO

• Clinical Research Associate

  • Jul 2007 - Jan 2009

  Inspecting and Review clinical study activities online to ensure compliance to SOPs and Good clinical Practices (GCP) and Good Laboratory Practices (GLP) Faced MCC, DCGI, UK Sponsors audit. Inspecting and Review clinical study activities online to ensure compliance to SOPs and Good clinical Practices (GCP) and Good Laboratory Practices (GLP) Faced MCC, DCGI, UK Sponsors audit.