Neo Life Sciences is a Hyderabad, India-based B2B pharmaceutical exporter sourcing WHO-GMP, EU-GMP, US-FDA, PIC/S, other SRAs certified APIs, Finished Pharmaceutical Formulations, Speciality and Complex therapeutics, Injectables and Hospital Products, Vaccines and Biologics, Nutraceuticals and dietary supplements, Medical devices and Diagnostics, Dermatology, Personal care and Cosmeceuticals.
Neo Life Sciences Pvt Ltd is a Hyderabad, India -based pharmaceutical merchant exporter, sourcing and supplying APIs, Finished Pharmaceutical, Specialty & Complex Therapeutics, Injectables & Hospital Products, Vaccines & Biologics, Nutraceuticals & Dietary Supplements, Medical Devices & Diagnostics, Dermatology, Personal Care & Cosmeceuticals, from certified Indian manufacturers to global markets.
Our Vision is to become a globally trusted pharmaceutical sourcing and export partner, improving access to quality healthcare across international markets.
We collaborate strictly with certified manufacturing laboratories holding WHO-GMP, PICS, EU GMP, US FDA , Other SRAs, ISO 9001:2015, and ISO 13485 accreditations. Every therapeutic batch, device shipment, and standardised extract is fully traceable back to its origin.
Our technical strength lies in our dedicated regulatory affairs department. We coordinate import licensing, MOH permit approvals, and compile complete product registration dossiers in Common Technical Document (CTD) formats to secure market entries swiftly.
Connecting global healthcare markets with trusted Indian manufacturers and quality-assured products.
Supporting international market requirements through reliable sourcing and regulatory solutions.
Creating seamless access to a broad range of Indian pharmaceutical and healthcare capabilities.
Building lasting business relationships through integrity, reliability, and excellence.
Temperature-controlled containers and real-time data loggers ensuring cold-chain integrity across international shipping routes.
We contract exclusively with globally audited manufacturers holding WHO-GMP, PIC/S, and EU-GMP accreditations with complete batch traceability.
Technical dossier filing, stability documentation, and MOH permit coordination to accelerate international market registration.
Founder & Managing Director, NEO LIFE SCIENCES PVT LTD
Prior to founding Neo Life Sciences, Mr. Eravathri spent over a decade running a successful IT staffing enterprise in the US, building deep expertise in cross-border business development, logistics, and international compliance.
A former Member of the Legislative Assembly (MLA) of Andhra Pradesh and Government Whip, his background provides unique policy insight, governance experience, and strong institutional relationships across India's industrial sectors.
Currently serving as the Chairman of the Telangana Mineral Development Corporation (TGMDC), he coordinates direct policy interfaces and possesses a strong grasp of regulatory standards for healthcare devices, manufacturing, and trade logistics.
Active Pharmaceutical Ingredients (APIs) and intermediates sourced from US FDA-inspected and WHO-GMP certified plants with comprehensive DMF filings.
WHO-GMP certified oral dosage forms including tablets, capsules, syrups, suspensions, and dry powders across all major therapeutic segments.
Critical care injectables, vials, ampoules, pre-filled syringes, and lyophilized products processed in aseptic cleanroom environments.
High-value branded generics and specialty therapeutics across oncology, cardiovascular, CNS, diabetes, and HIV/AIDS categories.
Premium nutraceuticals, vitamins, minerals, herbal supplements, and AYUSH-certified Ayurvedic formulations for global wellness markets.
CE, ISO 13485, and FDA-ready surgical instruments, diagnostics, hospital consumables, and healthcare disposables.
We guide pharmaceutical procurement cycles with complete accountability at every milestone.
Share your product list, target country, required volume, and any known regulatory requirements.
Our regulatory affairs team assesses country-specific compliance needs and delivers a quotation.
We prepare import permits, registration dossiers in CTD format, GMP certs, and COAs.
Verify GMP status, conduct batch documentation review, and confirm analytical testing.
Coordinate cold-chain freight (air/sea), handle customs clearance, and deliver complete docs.
Every export shipment includes WHO-GMP certificates, COA, COO, and technical dossiers compiled strictly in CTD format.
We contract exclusively with globally audited manufacturers, implementing full batch isolation and traceability for maximum quality control.
Get pricing quotations within 48 business hours and track dossier and shipping status transparently with a dedicated trade manager.
Temperature-tracked cold chain logistics and direct customs clearance to guarantee prompt, uninterrupted B2B supply lines.
Direct export & regulatory coordination from Hyderabad, India.