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

B.      GMP Auditing 

• 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