We at ArhamConsultants.com aim to serve and ease the complexities
in registration process by providing
resouceful knowledge and informed guidance
on the areas which have the greatest impact on procedural matters.

With the invaluable assets of priveleged information
our service areas are…

FOR MANUFACTURING IN INDIA

a. getting New Drugs Manufacturing permission for  Manufacturing in India any New Drugs / Fixed Dose Combination’s

b. Getting Approval / NOC for conducting Clinical trials &
Bio-equivalence studies.

c. getting Clinical Trials, Bio-Equivalance Study & Animal Toxicity Study
conducted  from reputed and approved Centers of DCGI.

d. getting CDL/CDTL/CIPL testing of bulk drugs and
imported formulations

FOR IMPORT INTO INDIA

e. getting Registration Certificate for the Manufacturing Premises and the individual MEDICAL DEVISES to be imported from the foreign manufacturers.

f. getting Registration Certificate for the Manufacturing Premises and the individual DRUGS AND FORMULATIONS to be imported from the foreign manufacturers.

g. getting Import Licence of Bulk drugs and Formulations

h. getting Test Licence for the purpose of examination, testor analysis.

FOR EXPORT FROM INDIA

i. getting Export Dosiers / Registration Documents made for registration of products in overseas markets.

j. getting Export Permissions for the export of Bulk drugs and Formulations

h. getting Export Documents Legalization from Buyer Country                 Embassy / Consulate.

Would you like to know more about us ?

If you would like to obtain more information about our services, please let us know. You can contact us by e-mail, phone, fax or by regular mail.