Galpha Laboratories Limited supply affordable and quality medicines across the globe, regardless of geographic and socio-economic barriers. This ability of ours can be ascribed to our successful portfolio of businesses, geographies and products.

Through our strong manufacturing services supported with highly qualified technical team we attempt to build blocks to produce an organization that manufactures therapeutics for a range of diseases.

We are committed to deliver healthy life to all strata of society and this endeavor of the company is supported by all employees. Motto of the company is to ensure Quality medicines at the most affordable prices.

We are manufacturers and exporters of range of Antibiotics, Multivitamins, Expectorants, Antacids, Analgesics and other general category products.

We aim to further strengthen our basket with specialized drugs like Antiretroviral, Pellets and Nutraceuticals. Today we are on the path of steady growth, striving for expansion into new markets including Europe and Middle East.

Galpha offer following services:

1.Contract R&D and product supply.
To develop formulation as per your requirement Carry out BE studies.
Carry out stability studies.
Develop registration dossier.
File for registration in European countries On registration, manufacture and supply commercial batches.
Analytical development Intellectual property (IP )
Well equipped modern Labs

Contract Manufacturing.
In case of an existing product We can undertake site variation procedure.
Take validation batches.
Generate stability data.
Manufacture and supply the product at competitive prices.

Patent challenge opportunities.
Work jointly on patent challenge opportunities in patented formulation.

2. Dosage forms & Technologies.
  • Film coated
  • Chewable tablets
  • Immediate Release Solid Dosage Form (IR)
  • Sustained Release tablet Technology
  • Dispersible tablets
  • Prolonged release
  • Delayed release
  • Effervescent Technology
  • Enteric Coated Technology
  • Direct Compression Technology

3.Regulatory Affairs.
  • highly qualified regulatory affairs team with masters/bachelors degree in pharmaceutical sciences.
  • RA is well versed with regulatory guideline of all major countries across the globe
  • RA is proficient in compiling of ANDA's, EU - CTD's & e CTD's
  • RA have a deep knowledge of registering the products in Europe through national, DCP, CP and MRP procedure
  • RA is adept at liasioning with various regulatory authorities and prompt in query handling for obtaining timely product approval / Marketing Authorization (MA's)


4.Intellectual property Management cell ( IPMC)
  • Galpha IPMC houses a well qualified and skilled team with technical expertise in pharmaceutics & Chemistry
  • Galpha IPMC is a adept in patentability analysis, filing national & international patent application and in prosecution of filed application
  • IPMC has personnel proficient in infringing analysis & validity analysis of third party patent
  • IPMC is an indispensable support for elucidation of R&D product pipeline and product filing strategies


Our group companies plant approvals
1) UK - MHRA
2) TGA - Australia
3) MCC - (South Africa)
4) WHO - GMP
5) Uganda
6) Malawi
7) Kenya
8) Ghana
9) Zimbabwe
10) Ivory coast
11) Ethiopia

Galpha's worldwide operation

EUROPE LATIN AMERICA CIS & RUSSIA AFRICA ASIA
Germany
U.K
Spain
France
Poland
Latvia
Lithuania
Estonia
Guatemala
Nicaragua
Peru
Jamaica
Azerbaijan
Belarus
Russia
Turkmenistan
Uzbekistan
Ukraine
Angola
Benin
Burkina
Faso
Central African Republic
Congo Democratic Republic Of Congo
Gabon
Ghana
Guinea
Conakry
Ivory Coast
Kenya
Malawi
Mozambique
Nigeria
Senegal
Tanzania
Togo
Uganda
Zambia
Mauritius
Sierra Leone
Liberia
Afghanistan
Cambodia
Myanmar
Philippines
Sri Lanka
Thailand
Vietnam