Pharmaceuticals, Cosmetic Consultancy
Located
in Abu Dhabi, Singapore, Kuwait, Dammam Saudi Arabia, Indonesia,
Maldives, Estonia, Tunisia, Albania, Mongolia, Sri Lanka, Egypt,
Turkey, Mauritius, Seychelles,Russia, Romania, Fiji Islands, South Africa, Israel, Tripoli - Libya, Iran, Jordan,Algeria,
Angola, Benin, Botswana, Burkina Faso, Burundi, Cameroon, Cape Verde,
Central African Rep., Chad, Congo, Congo, Dem. Rep., Cote d`Ivoire,
Djibouti, Egypt, Equatorial Guinea, Eritrea, Ethiopia, Gabon, Gambia,
Ghana, Guinea, Guinea-Bissau, Kenya, Lesotho, Liberia, Libya,
Madagascar, Malawi, Mali, Mauritania, Mauritius, Morocco, Mozambique,
Namibia, Niger, Nairobi, Nigeria, Rwanda, Sao Tome and Principe,
Senegal, Seychelles, Sierra Leone, Somalia, South Africa, Sudan,
Swaziland, Tanzania, Togo, Tunisia, Uganda, Zambia, Zimbabwe, Dubai, Abudhabi, Sharjah, Ras-al-khaimah, Fujairah, Um Al Quwain ,Abha,
Al-hasa, Al-Khobar, Baha, Dammam, Dhahran, Hail, Jeddah, Jizan, Jouf,
Jubail, Najran, Qassem, Qatif, Riyadh, Tabouk, Taif, Yanbu, Kurdistan,
South America, Europeun Union and looking for any of the below services
call 050 4773274
Looking
for Pharma Consultancy, Cosmetic Consultancy, API & Formulations
consultant ,USFDA consultant, TGA consultant, MHRA consultant, MCC
consultant, ANVISA consultant, EDQM consultant, ICH Q9 consultant, ICH
Q10 consultant, Cosmetic & Excipient consultant, EFFCI consultant,
cGMP consultant, Excipact consultant, Supply chain management
consultancy solution call +91 9845313910 or drop an email to shakti@gqsindia.com
I Pharmaceutical Industry (API & Formulations)
A. Document & Data preparation assistance
- Dossier/submission preparation or review and filing for various drug regulators worldwide.
· Submission preparation to other worldwide agencies in European Countries, South America, Australia, and Asia
· Consideration of international regulatory requirements
· Meeting international filings
· Revision of plans as guidelines change
- Facilitate
interaction with regulatory agencies, such as in meetings and
conference calls, negotiations during development stages,
submissions and submission approval process:
· Help you respond to regulatory agency questions
- Preparation
of your organization for USFDA /TGA/MHRA/MCC/ANVISA /EDQM etc .
GMP audits by gap analysis, document preparation, site specific
verification & guidance.
- ICH Q7a Gap Assessment
- Quality Risk management adequacy verification as per ICH Q9
- Help you establish quality systems in line with ICH Q10
II Cosmetic & Excipient Industry
· EFFCI (European Federation for Cosmetic Ingredients)
· ISO 22716:2007 Cosmetic cGMP compliance assistance
· EXCIPACT implementation assistance
· Gap audits and verification services to assist you in better system implementation
· Pharma, cosmetic, and excipient industry supply chain management solutions