'Oral dosage forms' presentation slideshows

Dissolution

Dissolution. Lynda Paleshnuik. Training workshop: Training workshop on regulatory requirements for registration of Artemisinin based combined medicines and assessment of data submitted to regulatory authorities, February 23-27, 2009, Kampala, Uganda. Overview.

2.38k views • 64 slides

EXTEMPORANEOUS PREPARATIONS BY SANA GHAYAS

EXTEMPORANEOUS PREPARATIONS BY SANA GHAYAS. LEARNING OBJECTIVES: At the end of this lecture, students will be able to: Know about extemporaneous dispensing. Define different dosage forms

5.85k views • 59 slides

Challenges - Risks of Single-use Systems

1.26k views • 54 slides

Bioequivalence studies: Regulatory Requirements on Conduct & Documentation of BE. Guidance & Experience.

1.51k views • 47 slides

Bioequivalence studies: Regulatory Requirements on Conduct & Documentation of BE. Guidance & Experience.

921 views • 47 slides

Bioequivalence studies: Regulatory Requirements on Conduct & Documentation of BE. Guidance & Experience.

1.16k views • 47 slides

Training Workshop on Pharmaceutical Development with focus on Paediatric Formulations Tallinn 15-19th October 2007

Pharmaceutical Development. Training Workshop on Pharmaceutical Development with focus on Paediatric Formulations Tallinn 15-19th October 2007. Pharmaceutical Development. Pharmaceutical Development of Finished Pharmaceutical Products (FPPs) Presenter: Susan Walters

602 views • 47 slides

WHO workshop on

WHO workshop on Quality, good manufacturing practice and bioequivalence with a focus on antituberculotics Jiaxing, China 5 to 9 November 2007. Comparative dissolution testing and applications. Theo Dekker, D.Sc. Research Institute for Industrial Pharmacy

754 views • 46 slides

TRAINING WORKSHOP ON PHARMACEUTICAL QUALITY, GOOD MANUFACTURING PRACTICE AND BIOEQUIVALENCE WITH A FOCUS ON ARTEMISININ

TRAINING WORKSHOP ON PHARMACEUTICAL QUALITY, GOOD MANUFACTURING PRACTICE AND BIOEQUIVALENCE WITH A FOCUS ON ARTEMISININS. Why are bioavailability / bioequivalence studies necessary? An Introduction to Bioequivalence Studies Presented by: Hans Kemmler, Consultant to WHO

592 views • 38 slides

Inventory Management

Inventory Management. Purchasing Systems Independent Purchasing: a single pharmacy entity establishes a contractual agreement with a pharmaceutical manufacturer or wholesaler. Group Purchasing: contractual agreement between a manufacturer or a wholesaler and a group of pharmacies

841 views • 32 slides

Prescription (Medical Prescription)

2.25k views • 30 slides

Bioequivalence Testing for Locally Acting Gastrointestinal Drugs: Scientific Principles

Bioequivalence Testing for Locally Acting Gastrointestinal Drugs: Scientific Principles. Gordon L. Amidon, Ph.D. Professor of Pharmaceutical Sciences College of Pharmacy The University of Michigan. Bioequivalence (BE): Orange Book.

805 views • 27 slides

Over View on the implementation of Repackaging Training.

Over View on the implementation of Repackaging Training. By: Jennifer Phelps, LPN/QMHP Central Virginia Community Services. Review Objectives. BOP Guidelines Re-Packaging Log Labeling of pillboxes Location where re-packaging can be done Facilitate Discussion.

412 views • 26 slides

PDR Electronic Library & Clinical Pharmacology Online:

PDR Electronic Library & Clinical Pharmacology Online:. Comparison & Evaluation for Collection Management Rae Jesano, MSLS, AHIP Health Science Center Libraries University of Florida. Reasons. Budget cuts Reassessed all subscriptions Electronic first Price increases PDR renewal due

515 views • 23 slides

Lessons Learned

Lessons Learned. Need for partnerships Need for an objective prioritization process Feasibility determination: frequency of use/condition defined for children Need for infrastructure, so that infrastructure is not the driver of feasibility. NIH Role. Prioritize therapeutic areas/drugs

377 views • 23 slides

SEMINAR ON Sublingual Drug Delivery System

SEMINAR ON Sublingual Drug Delivery System . List of contents 1. Anatomy physiology of mucosa 2. Sublingual tablets 3. Fast-disintegrating sublingual tablets 4. Bioadhesive sublingual tablet 5. Thin film drug delivery 6. Lipid matrix sublingual tablet

2.33k views • 20 slides

BCS-Based Biowaiver Monographs Prof. Dr. Jennifer Dressman & Corina Becker Johann Wolfgang Goethe University Frankfu

Dissolution, Pharmaceutical Product Interchangeability and Biopharmaceutics Classification. BCS-Based Biowaiver Monographs Prof. Dr. Jennifer Dressman & Corina Becker Johann Wolfgang Goethe University Frankfurt am Main, Germany. The WHO Biowaiver Procedure.

1.4k views • 17 slides

BCS-Based Biowaiver Monographs Prof. Dr. Jennifer Dressman & Corina Becker Johann Wolfgang Goethe University Frankfu

Dissolution, Pharmaceutical Product Interchangeability and Biopharmaceutics Classification. BCS-Based Biowaiver Monographs Prof. Dr. Jennifer Dressman & Corina Becker Johann Wolfgang Goethe University Frankfurt am Main, Germany. The WHO Biowaiver Procedure.

1.05k views • 17 slides

Bioequivalence studies for anti-malarials in the prequalification project: Outcomes and frequently encountered deficien

Bioequivalence studies for anti-malarials in the prequalification project: Outcomes and frequently encountered deficiencies. Overview and Examples . Hans Kemmler Consultant to WHO White Sands, 23.Aug. 2006. Summary of Submissions for Anti-Malaria Drugs (May 2006). Mono

345 views • 12 slides

Compressed tablets

Compressed tablets. Kelompok 1 (satu) Golongan Senin Laboratorium Teknologi Sediaan Padat Fakultas Farmasi Universitas Hasanuddin. Compressed tablets. Compressed tablets are the most widely used of all pharmaceutical dosage f orms for a number of reasons.

435 views • 12 slides