What We Offer
From dossier to dispatch —
complete pharma export services.
Three integrated capabilities that cover every stage of pharmaceutical export — regulatory affairs, merchant export, and market-entry support for Indian manufacturers.
3
Integrated service areas
100%
GMP-certified manufacturing partners
Service 01
Regulatory Affairs & Product Registration
Getting a pharmaceutical product registered in an emerging market is not a box-ticking exercise. Regulatory authorities in markets like Myanmar, Nigeria, Algeria, and Belarus have distinct requirements — different dossier formats, specific equivalence standards, and nuanced biowaiver criteria.
Healglobal prepares registrations that meet those requirements from the ground up. Dr. Gauri Chandrethiya leads every dossier strategy personally — applying pharmaceutical science, not just procedural knowledge, to each submission.
We work with both Indian manufacturers seeking to register their products in new markets, and overseas buyers who want an independently verified registration for their chosen product.
Who this is for
Overseas distributors who need product registered under their name or principal
Indian manufacturers entering a new export market for the first time
Buyers who have a product in mind but need registration clarity before committing
What we deliver
- Regulatory pathway assessment for target market
- CTD (Common Technical Document) dossier preparation
- ACTD (ASEAN Common Technical Dossier) preparation
- Q1/Q2 pharmaceutical equivalence analysis
- Q3 comparative dissolution profiling
- Biowaiver strategy and positioning
- Regulatory authority query response
- Product registration follow-up and liaison
- Post-approval variation management
- Drug Master File (DMF) coordination
Service 02
Merchant Export
As a licensed merchant exporter, Healglobal sources pharmaceutical formulations from Indian manufacturers and supplies them to overseas buyers — across eight therapeutic categories, spanning 15+ markets.
What separates Healglobal from a standard trading company is the quality filter. Every manufacturing partner we work with holds a recognised GMP certification — PIC/s, WHO-GMP, or EU-GMP. We do not source from uncertified facilities, regardless of price.
We also have the capability to supply Healglobal-branded products in markets where we hold registrations — giving buyers a supply option that comes with full regulatory coverage.
What buyers get
Access to GMP-certified Indian pharmaceutical manufacturing
Product sourcing across 8 therapeutic categories and 50+ SKUs
Healglobal-branded supply in registered markets
Full export documentation and logistics coordination
Regulatory alignment on product specs to match your market requirements
Therapeutic categories
Service 03
Export-Readiness for Manufacturers
For Indian pharmaceutical manufacturers who want to enter new export markets but lack the regulatory infrastructure or the international market knowledge to do it alone — Healglobal acts as a full export-readiness partner.
We work from the beginning: market selection, dossier preparation, regulatory submission, and — once the product is registered — can facilitate ongoing supply through our merchant export operations.
Manufacturers who work with us typically have one or more of the following situations: they hold WHO-GMP or PIC/s certification but have not registered outside India; they have attempted registration in a market but need stronger dossier support; or they want to evaluate whether their product portfolio is a viable fit for specific emerging markets.
Ideal for manufacturers who
Hold WHO-GMP, PIC/s, or EU-GMP certification
Have existing products but no international dossiers
Want to enter emerging markets without a dedicated export team
Need a regulatory partner, not just a trading agent
How it works
Market identification
We identify which markets are viable for your product — based on regulatory complexity, competition, demand, and your GMP certification level.
Regulatory pathway mapping
We map the exact regulatory requirements for your product in each target market — dossier format, reference product standards, biowaiver eligibility.
Dossier preparation
We prepare a market-specific registration dossier to the required CTD or ACTD standard — or adapt an existing dossier for the target authority.
Submission & follow-up
We manage the regulatory submission and handle all correspondence with the authority, including technical query responses.
Supply facilitation
Once registered, we can act as your merchant export channel — handling the supply relationship with the buyer and all export documentation.
How we work
One team. End-to-end.
Every engagement — regulatory question or sourcing request — is handled by the same team from first call to final shipment.
Discovery call
We understand your target market, product list, and regulatory baseline. No generic intake form — a real conversation.
Regulatory pathway
We map the exact dossier format, authority requirements, fees, and timeline for your target country.
Dossier preparation
CTD / ACTD compilation, Q1/Q2/Q3 analysis, biowaiver assessment, and translation where required.
Submission & tracking
We file with the national authority, manage queries, and track approval status — you get regular updates.
Approval & supply
Once registered, we can handle the export logistics, manufacturer coordination, and ongoing compliance.
Ready to start? Talk to us →
Let's talk
Have a market you're trying to enter? Or a product you need sourced?
Tell us what you're working on. We'll respond within one business day.
Talk to our regulatory team