MD Consultora shows up when manufacturers search for a Latin American registration holder or sanitary-registration partner. This article uses only what MD Consultora publishes on its own site (mdconsultora.pe/como-obtener-un-registro-sanitario), then compares it with multi-country market access from bioaccess®. It is a practitioner comparison, not a teardown.
What MD Consultora publishes
MD Consultora is a Peruvian consultancy that publishes a guide on how to obtain a registro sanitario. It offers dossier work and droguería setup, and in replies on the page says it can evaluate registering and importing through an already-constituted droguería. It does not have a dedicated holder product page.
MD Consultora vs bioaccess®
| Dimension | MD Consultora | bioaccess® |
|---|---|---|
| Public product | DIGEMID dossier + droguería setup | Registration, in-country holder, certified translations, tecnovigilancia as holder (import shipments quoted separately) |
| Geography | Peru | Published pricing in Mexico, Colombia, Brazil, Peru and Argentina; other markets quoted case by case |
| Public pricing | None published | Two-part: one-time registration fee per country by class, then an annual holder fee from year 2 (rate card) |
| Holder vs distributor | See the provider’s own terms | Holder under contract (own Colombian entity in Colombia; local partner elsewhere), with defined transfer provisions; the registration is never leverage |
| Bridge from a clinical trial | None published | Same firm can run the LATAM clinical trial and then hold the commercial registration |
Where each one fits
If you plan to set up your own Peruvian droguería, a consultancy that does droguería setup is the right first call.
bioaccess® market access is a different product. bioaccess® registers already FDA-cleared or CE-marked devices and acts as their registration holder under contract (in Colombia through its own Colombian entity; elsewhere with its local partner) across Latin American markets, including COFEPRIS, ANVISA, INVIMA, ANMAT, ISP and DIGEMID. Pricing is two-part pricing: a one-time registration fee per country by device class, then a lower annual holder fee from year 2 (published for Mexico, Colombia, Brazil, Peru and Argentina on the rate card). Importer-of-record shipments are quoted separately. The registration is held for the manufacturer’s benefit, with defined transfer provisions if you ever change partners or set up your own entity.
One country and one local partner is enough? Hire the firm that publishes that job. Several LATAM labels under one holder who is not your distributor? Start at bioaccess® market access, read the LATAM importer of record guide, try the market-access calculator, or request a registration quote.
Competitor facts from the MD Consultora public pages linked above, reviewed for bioaccess® competitive research (Aug–Oct 2026). Claims are theirs. No invented clients, prices or contacts.