GAYATRI GORE

30 K Connection's, Sourcing of Comparator Drug (RLD), API, Impurity, Dossier and Finished Formulation, Literature Support PV, Clinical Research Audit, Recruitment (Email: sourcing@tlifecare.com , techligament@gmail.com) @ TECHLIGAMENT LIFE CARE GROUP

About

Techligament Life Care Group is a Kalyan (Mumbai, India) We offer a complete solution to manufacturers, distributors, and procurement companies within the field of pharmaceuticals, clinical research, and biotech companies. We have Qualified CDMO-CMO-CRO Companies. Our partner CDMO-CMO -CRO is based in India offering products and services across all phases of a molecule’s lifecycle from development to commercialization. We innovate, co-create, and collaborate with Innovators and marquee pharmaceutical and specialty chemical companies to deliver high-standard products that enhance the quality of people’s lives with a strong focus on fundamentals such as ESG, quality, and compliance. Our CDMO-CMO-CRO Partner Company is Well Accreditations : · USFDA · UK MHRA · ANVISA · Health-Canada · DCGI · EU GMP · PMDA-JAPAN · WHO-GMP · KFDA-Korea · NMPA -China · Cofepris-Mexico We Provide Below Services : CDMO Services: Flexible and custom solutions for challenging development & and manufacturing needs. API + Formulations Services: Partner of choice for complex molecules AYURVEDIC and NUTRACEUTICALS PRODUCT: complex molecules CRO-Clinical and Analytical Services: High-class clinical solutions for Bioequivalence, Clinical Studies and Analytical Services A. Bio-equivalence –Clinical Studies: Independent Bioequivalence studies Monitoring services, Selection of CRO, Site, Bio-study outsource · Bioequivalence studies · Patient PK Studies · Clinical End-Point Studies · Clinical trials: Phase I to Phase IV · Nutraceuticals Studies · Clinical Data Management Platform · Post Marketing Studies for India & Global Market B. Global Comparator / RLD/ Innovator Products Sourcing from USA, UK, CANADA, France, Brazil, Japan, and Australia or Buy Back-RLD Expiry from the USA C. Medical Writing Services D. Full-Text Literature (Medical and Non-Medical Journals Articles) @200 + GST E. Translation Services F. Contract Research Manufacturing and Marketing and Distribution Services G. Regulatory Services like: H. Analytical Services USFDA approved facility in the USA and India Kindly send us your requirements. Regards Gayatri Dr Lalit Gore Mob No/WhatsApp No: +91-9167920553/ + 91 9167920552 Skype ID: Techligament Techligament Life Care Group For India Office: Mumbai, Maharashtra, India E: sourcing@tlifecare.com http://www.tlifecare.com

Country

India

City

Mumbai

Industry

Pharmaceuticals

Skill

RLD, Innovator Products, Branded Drug, Finished Formulation, Generic Drugs, Formulation Development, Dossier Sourcing, Analytical Skills, Impurities, working standard, metabolitoes, analytical testing, Clinical Trials, Pharmacovigilance, GCP, Clinical Research, Regulatory Affairs, Medical Writing, CRO, Biotechnology

Experience

Global Drug Sourcing Head

TECHLIGAMENT LIFE CARE GROUP

2011-7 - Present · 15 yrs 3 mos

Mumbai, Maharashtra, India

Your Support Welcome for below services: 1. Global Comparator / RLD/ Innovator Products Sourcing from USA, UK, CANADA, France, Brazil, Japan and Australia or Buy Back-RLD Expiry from USA • Single Batch Procure with long/Short expiry • Data logger, Controlled Shipment • Narcotic/Psychotropic RLD • REMS Products • Product is near to expiry product from The USA and after expiry 6 months only. 2. Medical Writing Services: • e-CTD Dossier • PSUR Preparation, • Clinical and Nonclinical Module 2, 4, 5 • Pharmacovigilance report, • Risk Management Plan, Abstract, • Manuscript Writing and Literature 3. Full-Text Literature (Medical and Non-Medical Journals Articles) @200 + GST and Translation Services 4. Contract Research Manufacturing and Marketing and Distribution Services • Third-Party Manufacturing finished Products and API • We will coordination for Marketing, Distribution Support all your products in Major Countries like USA, UK, EU, ROW countries like Nigeria, Ghana, Kenya, Rwanda, Uganda, Myanmar, Philippines, Cambodia, UAE, Saudi Arabia, Cameroon, Angola, Niger, Tanzania, Mozambique, Liberia, Madagascar, Burkina Faso, Ethiopia, Togo, Mali, Malawi, Burundi, Botswana, South Africa, Mongolia, Sri Lanka, Bangladesh, Malaysia, Vietnam, Uzbekistan, Tajikistan, Azerbaijan, Kyrgyzstan, Turkmenistan, Armenia, China, Hungary, Iran, Ukraine, Thailand, Romania, Kazakhstan, Indonesia, Georgia, Colombia, Egypt, Yemen, Syria, Russia, Zimbabwe. • Handled Dosage Form: Tablets, Capsules, Creams, Ointments, Solutions, Injections, Syrup, Powder, and Aerosols. • Accreditation Certificate: WHO Approved, USFDA, UK, WHO-GMP, MCC, ANVISA, and EU or PICS and ROW countries approved Plants 5. Bio-equivalence –Clinical Studies: Independent Bioequivalence studies Monitoring services, Selection of CRO, Site, Biostudy outsource • CRO / Site Identification for Bioequivalence and clinical studies