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Right to Information Act: Pharmaceutical Jurisprudence

Objectives

The basic object of the Right to Information Act is to empower the citizens, promote transparency and accountability in the working of the Government, contain corruption, and make our democracy work for the people in a real sense. It goes without saying that an informed citizen is better equipped to keep necessary vigil on the instruments of governance and make the government more accountable to the governed. The Act is a big step toward making the citizens informed about the activities of the Government.

Definitions

‘information” means any material in any form, including records, documents, memos, emails, opinions, advice, press releases, circulars, orders, and logbooks. contracts, reports, papers, samples, models, data material held in any electronic form, and information relating to any private body which can be accessed by a public authority under any other law for the time being in force

“public authority” means any authority or body or institution of self-government established or constituted—
(a) by or under the Constitution;
(b) by any other law made by Parliament;
(c) by any other law made by State Legislature;
(ci) by notification issued or order made by the appropriate Government,
and includes any—
(i) body owned, controlled, or substantially financed;
(ii) non-Government organization substantially financed, directly or indirectly by funds provided by the appropriate Government;

“record” includes—
(a) any document, manuscript, and file;
(b) any microfilm, microfiche, and facsimile copy of a document;
(c) any reproduction of image or images embodied in such microfilm (whether enlarged or not); and
(ci) any other material produced by a computer or any other device;

“right to information” means the right to information accessible under this Act which is held by or under the control of any public authority and includes the right to—
(i) inspection of work, documents, and records;
(ii) taking notes, extracts, or certified copies of documents or records;
(iii) taking certified samples of material;
(iv) obtaining information in the form of diskettes, floppies, tapes, video cassettes, or in any other electronic mode or through printouts where such information is stored in a computer or in any other device


Final Year B Pharm Notes, Syllabus, Books, PDF Subjectwise/Topicwise

Final Year B Pharm Sem VIIBP701T Instrumental Methods of Analysis Theory
BP702T Industrial Pharmacy TheoryBP703T Pharmacy Practice Theory
BP704T Novel Drug Delivery System TheoryBP705 P Instrumental Methods of Analysis Practical
Final Year B Pharm Sem VIIBP801T Biostatistics and Research Methodology Theory
BP802T Social and Preventive Pharmacy TheoryBP803ET Pharmaceutical Marketing Theory
BP804ET Pharmaceutical Regulatory Science TheoryBP805ET Pharmacovigilance Theory
BP806ET Quality Control and Standardization of Herbals TheoryBP807ET Computer-Aided Drug Design Theory
BP808ET Cell and Molecular Biology TheoryBP809ET Cosmetic Science Theory
BP810ET Experimental Pharmacology TheoryBP811ET Advanced Instrumentation Techniques Theory
BP812ET Dietary supplements and NutraceuticalsPharmaceutical Product Development

Suggested readings:

  • Create a database in MS Access to store the patient information
  • 20054 HPP Human Anatomy & Physiology Practical D Pharm
  • 20226 PLT Pharmacy Law & Ethics D Pharm
  • Education Regulations Pharmacy Act
  • Exporting Tables, Queries, Forms and Reports to web pages

Recommended readings:

  • Computer Applications in Pharmacy Practical

B Pharmacy Notes (Subjectwise/Topicwise)

  • F Y B Pharmacy Notes
  • S Y B Pharmacy Notes
  • T Y B Pharmacy Notes
  • Final Year B Pharmacy Notes
  • B Pharmacy All Subject Notes

D Pharmacy Notes (Subjectwise/Topicwise)

  • 1st Year D Pharmacy
  • 2nd Year D Pharmacy

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