By Express News Service
NEW DELHI: To tighten the manufacturing practices of pharma companies, the centre on Wednesday announced that those companies having more than Rs. 250 crores turnover will be given six months to adopt Good Manufacturing Practices (GMP), while those having less than Rs. 250 will be given 12 months for the same.
“This timeline for completion of GMP norms begins August 1,” Union Health Minister Mansukh Mandaviya said.
Schedule M of the Drugs and Cosmetics Act has not been implemented properly by the majority of the drugmakers, the minister conceded but said: “That is going to change now.”
He added that those who do not follow the timelines will be penalised according to the provisions of the law after two reviews are conducted — after six months and one year.
According to officials, there are around 10,500 manufacturing units in the country, of which around 8,500 fall under micro, small and medium-level enterprises, or MSMEs.
Schedule M of the Drugs and Cosmetics Act, 1940, deals with GMP for pharmaceutical manufacturing units, including specific requirements pertaining to premises, plant and equipment.
GMP are mandatory standards that bring quality into products by way of control on materials, methods, machines, processes, personnel and facility or environment, etc. GMP was first incorporated in Schedule M in 1988. The norms were last amended in 2018.
India is a major exporter of medicines to low- and middle-income countries which require GMP certification from the World Health Organisation (WHO), said a statement issued by the health ministry.
“We have around 2,000 units in the MSME category in the country having WHO GMP certification.”
In a statement, the union health ministry said that pharmaceutical manufacturing and the quality domain have developed significantly in the last 15-20 years
“Our understanding of the domain has increased because of development in pharmaceutical and manufacturing sciences…Linkage between manufacturing and product quality and interdependence between the two has been established.”
Observations from ongoing risk-based inspections further reiterated the need to relook at the current GMP regulations and quality management systems being followed by pharmaceutical manufacturers, it further said.
The statement said that drug regulators, as part of a drive to crack down on faulty drugmakers, inspected 162 units and 14 public testing labs over the last six months.
Major issues were detected during these inspections included poor documentation, lack of process and analytical validations, absence of self-assessment, absence of quality failure investigation, absence of internal product quality review, absence of testing of incoming raw material, infrastructural deficiency to avoid cross-contamination, absence of professionally qualified employees, faulty design of manufacturing and testing areas, the ministry said.
“Based on these factors and to keep pace with fast changing manufacturing and quality domain, there was a necessity to revisit and revise the principles and concept of GMP mentioned in current Schedule M. This would bring our GMP recommendations and compliance expectations at par with global standards, especially to those of WHO, and ensure production of globally acceptable quality of drug,” the statement said.
Accordingly, on the basis of discussion and recommendation of the Drug Technical Advisory Committee, a draft notification was issued in 2018 to upgrade and synchronise Schedule M of the Act with international standards.
Some of the major changes that will happen with the introduction of a revised Schedule M to support upgradation of the units are — introduction of Pharmaceutical Quality System (PQS), Quality Risk Management (QRM), Product Quality Review (PQR), qualification and validation of equipment, change control management, self-inspection and quality audit team, suppliers audit and approval, stability studies as per recommended climate condition, validation of GMP related computerised system, specific requirements for manufacturing of hazardous products, biological products, radiopharmaceutical and phytopharmaceuticals.
This will address most of the deficiencies related to documentation, failure investigation and technically qualified personnel with the right person doing the right job, the health ministry said.
“It will support the development of a robust quality management system in the company, thereby enabling the production of globally acceptable quality medicine. Better quality management will help manufacturers grow their business nationally and internationally, which is a huge opportunity for Indian pharmaceutical business,” statement added.
NEW DELHI: To tighten the manufacturing practices of pharma companies, the centre on Wednesday announced that those companies having more than Rs. 250 crores turnover will be given six months to adopt Good Manufacturing Practices (GMP), while those having less than Rs. 250 will be given 12 months for the same.
“This timeline for completion of GMP norms begins August 1,” Union Health Minister Mansukh Mandaviya said.
Schedule M of the Drugs and Cosmetics Act has not been implemented properly by the majority of the drugmakers, the minister conceded but said: “That is going to change now.”googletag.cmd.push(function() {googletag.display(‘div-gpt-ad-8052921-2’); });
He added that those who do not follow the timelines will be penalised according to the provisions of the law after two reviews are conducted — after six months and one year.
According to officials, there are around 10,500 manufacturing units in the country, of which around 8,500 fall under micro, small and medium-level enterprises, or MSMEs.
Schedule M of the Drugs and Cosmetics Act, 1940, deals with GMP for pharmaceutical manufacturing units, including specific requirements pertaining to premises, plant and equipment.
GMP are mandatory standards that bring quality into products by way of control on materials, methods, machines, processes, personnel and facility or environment, etc. GMP was first incorporated in Schedule M in 1988. The norms were last amended in 2018.
India is a major exporter of medicines to low- and middle-income countries which require GMP certification from the World Health Organisation (WHO), said a statement issued by the health ministry.
“We have around 2,000 units in the MSME category in the country having WHO GMP certification.”
In a statement, the union health ministry said that pharmaceutical manufacturing and the quality domain have developed significantly in the last 15-20 years
“Our understanding of the domain has increased because of development in pharmaceutical and manufacturing sciences…Linkage between manufacturing and product quality and interdependence between the two has been established.”
Observations from ongoing risk-based inspections further reiterated the need to relook at the current GMP regulations and quality management systems being followed by pharmaceutical manufacturers, it further said.
The statement said that drug regulators, as part of a drive to crack down on faulty drugmakers, inspected 162 units and 14 public testing labs over the last six months.
Major issues were detected during these inspections included poor documentation, lack of process and analytical validations, absence of self-assessment, absence of quality failure investigation, absence of internal product quality review, absence of testing of incoming raw material, infrastructural deficiency to avoid cross-contamination, absence of professionally qualified employees, faulty design of manufacturing and testing areas, the ministry said.
“Based on these factors and to keep pace with fast changing manufacturing and quality domain, there was a necessity to revisit and revise the principles and concept of GMP mentioned in current Schedule M. This would bring our GMP recommendations and compliance expectations at par with global standards, especially to those of WHO, and ensure production of globally acceptable quality of drug,” the statement said.
Accordingly, on the basis of discussion and recommendation of the Drug Technical Advisory Committee, a draft notification was issued in 2018 to upgrade and synchronise Schedule M of the Act with international standards.
Some of the major changes that will happen with the introduction of a revised Schedule M to support upgradation of the units are — introduction of Pharmaceutical Quality System (PQS), Quality Risk Management (QRM), Product Quality Review (PQR), qualification and validation of equipment, change control management, self-inspection and quality audit team, suppliers audit and approval, stability studies as per recommended climate condition, validation of GMP related computerised system, specific requirements for manufacturing of hazardous products, biological products, radiopharmaceutical and phytopharmaceuticals.
This will address most of the deficiencies related to documentation, failure investigation and technically qualified personnel with the right person doing the right job, the health ministry said.
“It will support the development of a robust quality management system in the company, thereby enabling the production of globally acceptable quality medicine. Better quality management will help manufacturers grow their business nationally and internationally, which is a huge opportunity for Indian pharmaceutical business,” statement added.
