We are Pharma Regulatory Service provider for various ROW countries and European countries. This is where we can help sponsors (companies) by our value added services. Oursubmission / dossier professionals generate this information from numerous sources including data management systems, medical writing departments, official pharmacopoeias, manufacturing sites etc. Once created, the documentation is compiled as dossier in standard formats like CTD, ACTD.
We have done work for following ROW Countries:
ALGERIA, ANGOLA, BANKOK, BENIN, BOLIVIA, BOTSWANA, CHILE, COLUMBIA,CONGO, COSTARICA, DOMINICAN REPUBLIC, DUBAI, GEORGIA, GHANA, HONKONG, GUATEMALA, IDA, KENYA, LEBANON, MACAU, MALI, MEDEK, MEXICO,
MOLDOVA, MONGOLIA, MOZAMBIQUE, MYANMAR, NEPAL, NIGERIA, PAKISTAN, PANAMA, PERU, PHILIPPINES, RUSSIA, SRILANKA, TAJIKISTAN, TURKMENISTAN, MAURITANA, THILAND, UGANDA, VIETNAM, ZAMBIA.
