Welcome to DPHARM GURU – Your Trusted Source for D Pharmacy Notes for 1st & 2nd Year.
D.PHARMACY NOTES: PART-1
D.PHARMACY NOTES: PART – 2
DPHARM GURU is a dedicated educational platform designed especially for D Pharmacy students across India. Here, you’ll find clear and exam‑oriented D Pharmacy notes for both 1st and 2nd year, along with subject‑wise study materials based on the latest PCI D.Pharm syllabus. Our goal is to make it easy for you to access all important topics, units and chapters in one place.
Whether you are in the 1st year or 2nd year of your D.Pharm course, our D Pharmacy notes help you understand concepts faster and revise more effectively before exams. Each topic is carefully simplified using student‑friendly language, covering key subjects like Pharmaceutics, Pharmacognosy, Pharmaceutical Chemistry, Human Anatomy and Physiology, Health Education & Community Pharmacy, and more. You can use these notes for daily study, class tests, sessionals and final university exams.
DPHARM GURU also provides additional D.Pharm study resources such as important questions, previous year question patterns and chapter‑wise summaries to support your exam preparation. All notes are arranged in a structured, subject‑wise and year‑wise format so you can quickly find what you need without wasting time.
Our mission is to help every D Pharmacy student study smarter with reliable notes, updated syllabus content and free, high‑quality study material. Start exploring our D Pharmacy notes today and make your D.Pharm exam preparation easier, faster and more confident with DPHARM GURU
- 21. MEDICAL DEVICES
MEDICAL DEVICES A medical device is any instrument, device, implement, machine, appliance, implant, in vitro reagent, software, material, or other similar or related item that the manufacturer intends to use for a medical purpose, either alone or in combination. There are 22 notified medical devices under the Drugs & Cosmetics Act, 1940, which need to… Read more: 21. MEDICAL DEVICES - 20. INTRODUCTION TO THE DISASTER MANAGEMENT ACT
DISASTER MANAGEMENT ACT, 2005 The Government of India passed the Disaster Management Act, 2005 (DMA 2005) on 23 December 2005. The prime purposes of introducing this act are: 1) To ensure the efficient management of disasters; and 2) To deal with matters linked to disasters. This act came into the news with the onset of… Read more: 20. INTRODUCTION TO THE DISASTER MANAGEMENT ACT - 19. INTRODUCTION TO THE CONSUMER PROTECTION ACT
CONSUMER PROTECTION ACT, 2019 Earlier, the protection of rights and interests of consumers was governed by the Consumer Protection Act, 1986. However, due to some flaws in the Act with respect to the changed scenario, the existing Act was required to be replaced by a new Act. Consequently, a new bill for the Consumer Protection… Read more: 19. INTRODUCTION TO THE CONSUMER PROTECTION ACT - 18. BIOETHICS
BIOETHICS Bioethics is the discipline dealing with the ethical implications of biological research and application, especially in medicine. It includes the study of what is right and wrong in new discoveries and techniques in biology, such as genetic engineering and organ transplantation. The term Bioethics (Greek bios = life; ethos = behavior) was coined in… Read more: 18. BIOETHICS - 17. BIOMEDICAL WASTE MANAGEMENT RULES 2016
BIOMEDICAL WASTE MANAGEMENT RULES, 2016 Biomedical Waste Management Rules, 2016 (BMWM) was issued by the notification of the Ministry of Environment, Forestry, and Climate Change in March 2016 stating that every healthcare facility must take all necessary efforts to guarantee that biological waste is managed safely and without causing harm to human health or the… Read more: 17. BIOMEDICAL WASTE MANAGEMENT RULES 2016 - 16. CLINICAL ESTABLISHMENT ACT AND RULES
CLINICAL ESTABLISHMENT ACT AND RULES On 17th August 2010, the Clinical Establishments Act was passed by the Indian Parliament to provide for the registration and regulation of all clinical establishments in the country, with the goal of recommending minimum standards of facilities and services offered by them, in order to fulfil the mandate of Article… Read more: 16. CLINICAL ESTABLISHMENT ACT AND RULES - 15. BLOOD BANK
BLOOD BANK Blood banking is a process carried out in the laboratory to ensure that donated blood or blood products are safe to be used in blood transfusions and other medical procedures. Blood is collected and divided into its many components by blood banks so that it can be efficiently used based on patient’s needs.… Read more: 15. BLOOD BANK - 14. INTRODUCTION TO BCS SYSTEM OF CLASSIFICATION, BASIC CONCEPTS OF CLINICAL TRIALS, ANDA, NDA, NEW DRUG DEVELOPMENT, NEW DRUGS AND CLINICAL TRIALS RULES, 2019
BCS SYSTEM OF CLASSIFICATION Biopharmaceutics Classification System (BCS) is a fundamental guideline for determining the conditions under which In-Vitro In-Vivo Correlations (IVIVC) are expected. BCS is also used as a tool for developing in-vitro dissolution specifications. BCS Drug Classification Class Solubility Permeability Rate Limiting Step Bioavailability Class I High High Dissolution & absorption very fast… Read more: 14. INTRODUCTION TO BCS SYSTEM OF CLASSIFICATION, BASIC CONCEPTS OF CLINICAL TRIALS, ANDA, NDA, NEW DRUG DEVELOPMENT, NEW DRUGS AND CLINICAL TRIALS RULES, 2019 - 13. GOOD REGULATORY PRACTICES
GOOD REGULATORY PRACTICES (GRP) Good Regulatory Practices (GRP) are processes, systems, tools, and methods for improving the quality of regulations that are internationally recognised. Before government initiatives are implemented, GRP systematically implements public consultation and stakeholder involvement, as well as impact analysis of government proposals to ensure they are fit for purpose and will achieve… Read more: 13. GOOD REGULATORY PRACTICES
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“DPHARM GURU is an educational platform for pharmacy students based on the PCI syllabus. The study materials, notes, and drug information provided here are strictly for academic and exam preparation purposes. Content on this site must not be used as medical advice, diagnosis, or treatment.”