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PHARMACY COUNCIL OF INDIA STANDARD INSPECTION FORM HARM. D and HARM. D (POST BACCALAUREATE) (To be filled and submitted to PCI by an organization seeking approval of the Course /continuation of the
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01
To fill out Form D, you need to provide your personal and contact information, including your name, address, and phone number. You also need to provide information about the securities you are offering, such as the type of security, the offering price, and any commissions or fees involved. Additionally, you will need to disclose information about your business and its management team.
02
To fill out Form Pharm, you need to provide detailed information about your pharmacy, including its name, address, and contact details. You will also need to provide information about the pharmacist-in-charge, including their name, license number, and contact information. Additionally, you will need to provide information about the type of pharmacy you operate and any additional services you offer.
Who needs d and pharm?
01
Individuals or companies who are offering securities to the public need to fill out Form D. This includes entities such as startups, small businesses, and investment funds.
02
Pharmacy owners or operators who are seeking to obtain or renew a pharmacy license need to fill out Form Pharm. This includes retail pharmacies, hospital pharmacies, compounding pharmacies, and specialty pharmacies.
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What is d and pharm?
The terms 'd and pharm' refer to the declarations and pharmacovigilance reports required by regulatory authorities.
Who is required to file d and pharm?
Manufacturers, marketers, and distributors of pharmaceutical products are typically required to file d and pharm.
How to fill out d and pharm?
D and pharm reports can be filled out electronically through the specified regulatory authorities' online portals.
What is the purpose of d and pharm?
The purpose of d and pharm is to ensure the safety and efficacy of pharmaceutical products on the market.
What information must be reported on d and pharm?
Information such as adverse reactions, medication errors, and product defects must be reported on d and pharm.
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