First Register 

The first register is prepared by the State Government under the Pharmacy Act, 1948. 

The first register includes -

  1. The full name and residential address of the registered person, 
  2. The date of his first admission to the register, 
  3. Tis qualifications for registration, 
  4. His professional address etc. 
- There are Various qualification criteria for a person to enter his name in the first register. 

Subsequent Register 

The Subsequent Register is prepared after the First Register and before the Education Regulations have taken effect in a state. 
A person desirous of having his name registered in the Subsequent Register has to qualify for the following particulars:
  1. Should be at least 18 years of age.
  2. Should have paid the prescribed fee

Removal of Name From Register:

The names of the registered persons may be removed from the register on the following reasons: 
  1. If his name has been entered into the Register by error, misrepresentation
  2. A person who gives false information about himself/herself.
  3. A person who submits false certificate or false document in support of his/her registration. 
  4. A person who is convicted of an offence in connection with his/ her profession. 
  5. A person who was indirectly involved in the commitment of a professional offence and if it is proved that the offence was instigated or connived at by the registered pharmacist. 
Any person aggrieved by the order for removal of his name from the register may appeal within 30 days from the communication to him of confirmation of the order by the State Council and the State Government decision is final. 

A person whose name has been removed from the register has to surrender his registration certificate to State Pharmacy Council Registrar and the name so removed is published in the Gazette. 

Comments

Post a Comment

Popular posts from this blog

Image
Manufacture of New Drugs:  As per the Rule: A new drug can be a new substance of chemical or biological origin; in bulk or prepared dosage from; used for prevention, or treatment of disease in human or animal which is not used in the country except the clinical Trial  If the ratio of ingredients is in an already marketed combination must be changed with certain factors like- Indications  Dosage from  Route of Administration  All vaccines are new drugs unless certified by the licensing authority.  A drug is said to be a new drug for about 4 years from the date of tits approval.  Loan License:  It is issued by a licensing Authority to a person who do not have any manufacturing license.  A separate license may be issued for the sale of drug more than 1 place.  Before the grant of license the license authority must satisfy the conditions for the grant of license like the manufacturing unit must have enough staff and components for manufacture.  For the manufacture of drugs more than 10 ite
Read more
General Labelling Requirements The following particulars shall be either printed or written in indelible ink and shall appear in a conspicuous manner on the label of the innermost container of any drug and on every other covering in which the container is packed: 1. Drug name: the proper name of the drug shall be printed or written in a more conspicuous manner than the trade name, if any. 2. Net content: weight, volume, in metric system or units. 3. Content of Active ingredients: Oral liquids: Contents per single dose, i.e. 5 ml or multiple thereof. If dose is below 5 ml, then per ml. Liquid parenterals: Contents per ml or in percentage or per dose. Solid parenterals: Contents per mg or per gm or in terms of units. Tablets, capsules and pills: Contents per tablet, capsule, pill. For other preparations: Contents in terms of percentage by w/w or w/v or units per gm or ml. 4. Name and address of manufacturer. 5. Manufacturing license number: Mfg. Lic. No. or ML No. 6. Batch number: Batc
Read more
Conditions of license for the manufacture of Schedule C, C1 and X drugs  Following are the general conditions for the manufacture of schedule C, C1 and X drugs; License Must - 01 Provide and maintain staff, premises and equipments as per schedule M and M3 02 Test raw materials and final products of each batch by licensing authority. 03 Maintain records of Manufacturing and Testing of each batch. 04 Allow drug inspector to enter to inspect the premises and conduct the essential tests. 05 Allow drug inspector to check the registers and records. 06 Time to time report to the licensing authority about the (i)               Changes in staff (ii)             Alterations in material (iii)           Samples of Drugs 07 Not sell any batch until the licensing authority gives permission 08
Read more