Schedule A -
Proforma for application for the licenses, issue and renewal of licenses for
sending memorandum under the Act - .
Schedule B -
Rates of fee for test or analysis by the Central Drugs Laboratory ' or the Government
Analyst. ‘ _ . .
Schedule C -
List of biological and special products whose import, sale, distribution
and manufacture are governed by Special provisions
Schedule CI -
List of other Special products whose import,
sale distribution
and manufacture are governed by special provisions
Schedule D--
List of drugs exempted from the provision of Import of drugs
Schedule: E - List of poisonous substances under the
Ayurvedic (including Sidha) and Unani systems of
medicine.
Schedule F
(I) Space, equipment and supplies
required for a blood bank.
(ii) Minimum requirement for grant of license to procure blood components
from whole human blood.
Schedule F,
Part I --
Provisions applicable to the
production of bacterial and viral vaccines,
Part II- Provisions applicable to the production of all sera from living animals.
Part III - Provisions applicable to the manufacture and standardization of diagnostic agents
(bacterial origin).
Schedule F2 --- Standards for surgical dressings.
Schedule F3 - Standards for sterilized umbilical tapes.
Schedule FF - Standards for ophthalmic
preparations.
Schedule G List of substances that are required to
be used only under medical supervision and which are to be labeled accordingly.
Schedule H- List of prescription drugs.
Schedule J - Diseases or ailments which a drug may not purport to prevent
or cure.
Schedule K- Drugs exempted from certain provisions
relating to the manufacture of drugs.
Schedule M- Good Manufacturing Practices (GMP)
requirements of factory premises, plants and equipment
Schedule M1 - Requirements of factory premises etc for
manufacture of homeopathic preparations.
Schedule M2 —Requirements of factory premises for
the manufacture of cosmetics. Requirements of factory premises for manufacture
of medical
Schedule N- List of minimum equipment for efficient
running of a pharmacy.
Schedule 0 - Standards for disinfectant fluids
Schedule P- Life periods of drugs
Schedule P1- Pack sizes of drugs
Schedule Q
Part I - List of dyes, colors and pigments permitted in cosmetics and soaps.
Part II- List of colours permitted in soaps.
Schedule R Standards for condoms made of
rubber latex intended
for single use and other mechanical contraceptives.
Schedule R, Standards for medical devices.
Scheule S- Standards for cosmetics.
Schedule T- Requirements of factory premises and
hygienic conditions for Ayurvedic ("including Sidha) and Unani of drugs,
Schedule U- Particulars to be shown in manufacturing, raw material and analytical
records of Drugs
Schedule
U1- Particulars to be shown in manufacturing, raw
material and analytical cords of cosmetics
Schedule
V- Standards for patent or proprietary medicines
Schedule W List of drugs which are to be marketed under generic
names only
Schedule X List of drugs whose import, manufacture and sale
lebelling and packaging are governed by special provisions.
Schedule Y Requirements and guidelines on clinical trials for import and
manufacture of new drugs
Comments
Post a Comment