www.iso-consultancy.com

 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 050 4773274 or drop an email to This e-mail address is being protected from spambots. You need JavaScript enabled to view it

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

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