All regulatory bodies has the responsibility to
provide access to the safe, effective and quality, medication to their
people. The Central Drugs Standard
Control Organization and Drug Controller General of India are bequeathed to
protect the citizens from the exposer of unsafe medication. Either it is
through clinical research or marketing. The growing clinical research after the
product patents rights for the pharmaceutical industries as per the trade
related aspects of intellectual property rights agreement and adverse drug
reaction monitoring, rights and safety of Patients, compensation after adverse
event clinical research and of the marketed drugs have raised many ethical and
regulatory issues.
The regulatory measures has to be dynamic and ever
evolving in consonance with the developing technologies. Indian regulations have also experienced this a lot of change from british era. Last three years were little disturbing and this lead to loss of opportunity and mistrust in Pharmaceutical domain. But now regulation is well organized, systematic and compliant
to international regulatory standards for pharma products, medical devices,
traditional herbal products and cosmetics.
Now question arise why Indian regulators took so
much time in this reform? To understand this we have to understand the history
of Clinical research. It started in British Raj when most of the drugs were
imported from foreign countries. Post First World War, the demand for drugs had
increased tremendously and that led to the cheap, substandard, spurious and
adulterated drugs into the market. To control in market, Government passed the
Poisons Act 1919. This Act regulates possession of substance or sale of
substances as specified as poison. The Poisons Act was followed by The
Dangerous Drugs Act 1930. This act regulates the opium plant cultivation,
manufacture and possession of opium, its import, export, tranship and sell of
opium.
In response to widespread ‘Gigantic Quinine Fraud’;
the Government, then, formed a Drug inquiry committee under Sir Ram Nath Chopra
also known as ‘Chopra Committee’ whose recommendations later on tabled amidst
growing protest in legislative assembly as ‘The Drug Bill’ later on amended to
the Drugs and Cosmetic Act 1940 (D and C Act) and Drugs and Cosmetic rules of
1945. This also established the Central Drugs Standard Control Organization
(CDSCO), and the office of its controller, the Drugs Controller General (India)
(DCG(I)). The CDSCO in the Directorate
General of Health services, is a division in Ministry of Health and Family
welfare, Government of India, headed by Drug Controller General of India (DCGI).
It has four zonal, three sub-zonal and seven port/airport offices and six
laboratories to carry out its activities. The Drugs and Cosmetic Act, 1940 came
into force from 1st April 1947. In year 1948 Pharmacy Act came into existence
to regulate the profession of pharmacy in India and in 1955 Drugs and Magic
Remedies rule came into existence for control the claim and advertisement.
In 1962, government extended the regulatory
provisions to the cosmetics, and finally the Act came to known as Drugs and Cosmetic
Act 1940. Drugs and Cosmetic Act has been divided in Chapters, Rules and
Schedules and is amended from time to time to control the safety, efficacy and
quality of the drugs. It is an act to regulate the import, manufacture,
distribution and sale of the drugs and cosmetics. Manufacture and sale is under
the respective states governments and union territories through their
respective drug control organization, whereas setting standard, import,
marketing authorization and monitoring of adverse drug reactions of a new drug
is under Central Government. Under Chapter Two of this Act, one statutory board
and a committee have been framed called Drugs Technical Advisory Board (DTAB)
and Drug Consultative Committee (DCC) separately for Modern Scientific System
of Medicine and Indian traditional system of Medicine and a provision of
Central Drug Laboratory at Central Research Institute, Kasauli for testing
drugs has been made in this act. DTAB comprises of technical experts who
advises central and state governments on technical matters of Drug regulation.
Amendment, if any, to Drug and Cosmetic are made after consulting this board.
During this period the market share was dominated
by multinational companies and very few Indian manufacturers were present. The
Indian Pharmaceutical industry was in an early stage of growth. Focus for pure
research and development was very little due to lack of patent protection. Due
to very high import dependency on drugs, the cost of drugs was very high as
well as market availability was comparatively low. In 1955, government has
passed Drugs Prices Control Order, 1955 (DPCO) (under the essential commodities
Act). Due to which many essentials drugs were unavailable in Indian market. To
save Indian companies and to provide medicine Indian population at low cost Indian
government introduced Indian Patent Act of 1970. This new act replaced the
Indian Patents and Designs Act of 1911.
The Indian Patents Act of 1970 originally had
provisions for ‘process’ patents only. Now, local companies began manufacturing
products/ drugs using different manufacturing process by reverse engineering.
Due to this new drugs were available cheaply as well as many more substitute
drugs were available in the market against costly imported new drugs. This has
resulted in 1) increase the exports to countries like Russia, Africa, China,
and South America. 2) Export of Bulk drug post patent expiry.
In 1994, Government signed the agreement on Trade
Related Aspects of Intellectual Properties (TRIPS) to provide minimum
protection to the Intellectual Property by the member states of World Trade
Organization (WTO). India amended the Patent (Amendment) Bill before 2005 and
extended its weak process patent to strong TRIPS competent ‘Product’ patent
system for pharmaceutical products.
The Indian government, realizing the potential of
clinical research for new therapies, has modified and amended Schedule Y to the
Drug and Cosmetics Rules of 1945. Schedule Y establishes a set of guidelines
and requirements for clinical trials. However, Schedule Y was written with the
generics industry in mind but increase entry of foreign pharmaceutical
companies after the introduction of strict patent rules in the area of clinical
research led the government to introduce many changes. The government
recognized the importance of their regulation and thus developed Ethical and
Regulatory Guidelines. The Indian Council of Medical Research (ICMR) issued the
Ethical Guidelines for Biomedical Research on Human Subjects in 2000 and CDSCO
released Indian Good Clinical Practice (GCP) guidelines in 2001.
With the application of Product patent in 2005,
recognizing individual's innovations through the Trade Related Aspects of
Intellectual Property Rights (TRIPS) agreement, which India had signed in 1995,
became effective. Indian companies began to respect Intellectual Property
rights, consistent with international standards. With the increasing faith in
the system, companies flooded the market and more global trials came. Lately,
to decrease the review time of application from 16 weeks to 10 weeks the CDSCO
has introduced the fast tracking of clinical trials in 2006. The DCG (I)
created two categories of applications; Category: (A) Those also being
conducted in countries with competent, mature regulatory systems, and Category:
(B) Everything else.
Trials that fell into category A (received approval
in the U.S., Britain, Canada, Germany, South Africa, Switzerland, Australia,
Japan and countries in the European Medicines Agency (EMEA)) would be eligible
for fast tracking in India, with approval taking no more than two to four
weeks. Trials in category B would fall under more scrutiny; with approval
taking 12 weeks once an application is considered under Category B, it, in any
case, cannot be shifted to Category A. Nearly all global trials are in the
Category A.
In 2011, Drugs and Cosmetics (First Amendment)
Rules was implemented. It mandates registration of Clinical Research Organization
(CRO) for conducting Clinical Trials (CT). Schedule Y suggests requirements and
guidelines for registration of Clinical Research Organizations. Although
amendment to Schedule Y, registration of Contract Research Organizations,
registration of Clinical Trials, Speeding up review process, Pharmacovigilance
(PV) programme for India and Inspection of clinical trial sites have been
started. However due to casual approach in marketing approval, unethical steps
taken by some pharmaceutical companies and medical practitioners has reiterated
the need to amend the regulations. DCGI slowed down their actives related to
approval of studies as per the guidance of Supreme Court and Government of
India and started concentrating on the regulatory framework.
DCGI further amended the policies for to improve
the quality of clinical research. It took three years to design this:
- Sponsors, investigators, the regulator and Ethics Committees are responsible for ensuring that the design of placebo-controlled trials is appropriate, efficient and ethical;
- The Ethics Committees will have to be registered under DCGI
- Investigators are limited to working on a maximum of three trials simultaneously;
- If a new chemical entity is approved in the innovator or “well-regulated” country for a disease prevalent in India, and the clinical trial included Indian participants, CDSCO advises that “approval should be sought from CDSCO” and “these NCEs should be marketed in India speedily.” CDSCO also specifies that if a foreign trial included Indian participants, the number would have to be “adequate” for considering approval of the drug in India;
- Waiver of clinical trials in Indian populations with drugs already approved outside India will only be considered in cases of national emergency, extreme urgency and epidemic, and for orphan drugs for rare diseases and drugs for conditions/diseases for which there is no therapy;
- Generics and biosimilars marketing “in other countries like USA” for over four years and have a “satisfactory report” can be approved in India after abbreviated trials;
- Consideration of new drug applications will take into account ethnic differences in metabolism etc.;
- If two or more countries remove a drug from their market on the grounds of safety and efficacy, the continued marketing of the drug in India “will be considered for examination and appropriate action” by CDSCO; and
- Manufacturers, sponsors and CROs are advised to provide compensation for any drug-related anomaly detected at a later stage.
- CDSCO is also re-organizing the structure of the committees involved in the drug approval process. The New Drug Advisory Committees will now become the Subject Expert Committees, whose recommendations will be reviewed by a newly formed Technical Review Committee (TRC). The TRC will be under the direction of the Directorate General of Health Services (DGHS), which will draw the membership of the committee from experts in such areas as clinical pharmacology, clinical toxicology/ pathology, and scientists involved in drug development.
As we all understand that regulatory improvement is
continual process and no system is perfect. DCGI still needs a lot of
improvement to ensure safety and wellbeing of Indian population along with
promoting introducing new product.
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