Neo Ayushveda Pvt Ltd is a specialist pharmaceutical trader and exporter, sourcing WHO-GMP certified generics, medical devices and herbal formulations from India's finest certified manufacturers — delivering them to regulated healthcare markets across every continent.
Neo Ayushveda is a specialist B2B pharmaceutical trading and global export partner based out of India's healthcare innovation hub, Hyderabad. Rather than operating raw manufacturing assets, we act as a streamlined sourcing catalyst for regulated international markets.
We collaborate strictly with certified manufacturing laboratories holding WHO-GMP, ISO 9001:2015, and ISO 13485 accreditations. Every therapeutic batch, device shipment, and standardized 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.
Sourcing WHO-GMP generic formulations, oncology products, and custom injectables from certified facilities.
CE and ISO 13485 compliant clinical diagnostics, surgical equipment, and rehabilitation hardware.
AYUSH-certified classical organic extracts, dietary nutraceuticals, and functional wellness cosmetics.
Cold-chain air cargo and shipping logistics with complex customs clearing and dossier registration support.
Founder & Managing Director, Neo Ayushveda Pvt Ltd
Prior to founding Neo Ayushveda, Mr. Eravathri spent over a decade running a successful IT staffing enterprise in the United States, building deep organizational expertise in cross-border business development, corporate logistics, and international regulatory compliance.
A prominent public figure, he is a former Member of the Legislative Assembly (MLA) of Andhra Pradesh and served as Government Whip. This background brings a unique combination of administrative policy insight, governance experience, and strong institutional relationships across India's industrial sectors.
Currently serving as the Chairman of the Telangana Government Mineral Development Corporation (TGMDC), Mr. Eravathri coordinates direct policy interfaces and possesses an unparalleled grasp of regulatory standards for healthcare devices, clinical manufacturing, and trade logistics.
Sourcing prescription generic medicines across all major therapeutic categories (HIV/AIDS therapeutics, oncology, cardiovascular, CNS) from WHO-GMP certified facilities.
Exporting therapeutic solutions including oncology treatments, diabetes care, HIV/AIDS, tuberculosis (TB), critical care medicines, cardiovascular care, injectables, vaccines, and daily nutraceuticals.
Premium daily health supplements, vitamins, multi-minerals, and organic nutrient formulations for international health markets.
We found all pharmaceuticals for Anti Diseases, Critical care injectables, vials, pre-filled syringes, and high-safety vaccines processed under strict aseptic cleanroom environments.
Active Pharmaceutical Ingredients, bulk drug actives, and regulatory intermediates sourced from US FDA-inspected manufacturing plants.
CE, ISO 13485, and FDA-ready surgical instruments, diagnostic equipment, healthcare disposables, and clinical hardware.
Classical Ayurvedic formulations, natural wellness vatis, churnas, and tailas sourced from licensed AYUSH GMP manufacturers.
Standardized organic botanical extracts, phytochemical actives, and custom herbal capsule ingredients with complete batch COAs.
Dermatologist-recommended skincare, clinical haircare, and personal wellness cosmetics available with Halal or Vegan certifications.
Exporting raw materials, bulk drug formulations, and high-purity chemical substances to global pharmaceutical manufacturers.
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.
We don't just source — we document. Every export shipment includes WHO-GMP certs, Certificate of Analysis (COA), Certificate of Origin (COO), and dossiers compiled strictly in CTD format.
We contract exclusively with licensed manufacturers audited by global bodies. We implement complete batch isolation and traceability to prevent quality bottlenecks.
Get pricing quotations within 48 business hours. Track regulatory dossier status and shipping configurations transparently via a dedicated international trade manager.
Streamlined global logistics with temperature-tracked cold chain support and direct customs clearance to guarantee prompt, uninterrupted B2B supply lines.