Important international organizations and guidelines concerned with clinical trials are WHO, ICH and FDA Guidance . NIH ClinRegs is global information database of 20 countries.
Guidelines and regulations from pharma and healthcare sectors. Official Guidelines, rules and regulations presented in easy to understand way. Clinical trials, patent , manufacturing, business etc.
Find all important cosmetics GMP Guidelines Here. ISO 22716 is most adopted standard worldwide for cosmetics GMP. USFDA, EC Regulations are also important.
Schedule M-3 specify GMP requirements for premises such as buildings, equipment, design and development validation, record keeping etc for medial devices and diagnostic products.
The GMP requirements in schedule M1 are for Cosmetic Products. It specify GMP requirements for premises such as buildings, equipments, basic sanitation etc for cosmetic products.
Schedule M 1 explains the GMP requirements for Homeopathic industry in India. Potentiation section, lotions section, opthalmic preparation section etc.
Schedule M has 6 parts. It specify GMP requirements for pharmaceutical products. Buildings, air conditioning, waste management, sanitation of workers and record keeping etc.
Schedule M, M1, M2, M3 are parts of Drugs And Cosmetics Act. They Contain GMP for Drugs such as pharmaceuticals, Cosmetics And Medical Devices.
In march 2019 Pharmacist recruitment rules are changed in Delhi. Now B. Pharm is the minimum qualification required for the government pharmacist job in Delhi.
The new Rules have been framed in conformity with Global Harmonisation Task Force (GHTF) framework. The salient features of Medical Device Rules 2016 Rules are: