Bioforum - Applied Knowledge Center

23/05/2013 #C13505

תפקידו של ה QP הקליני בעקבות אישור נוהל משרד הבריאות

27/05/2013 #13387

Effective Quality Risk Management & CAPA A GMP Inspector’s Perspective on Compliance

27/05/2013 #13628

Solid Oral Dosage Forms- Smart Design of Formulations

28/05/2013 #13437

Preparing For and Passing an FDA Inspection

28/05/2013 #13240

GC Applications - Advanced Course for Managers

29/05/2013 #13454

International GMP for Cosmetics

29/05/2013 #13097

Protein Analysis by MS

03/06/2013 #13476

Suppliers Evaluation

03/06/2013 #13613

Medical Device - First in Man

03/06/2013 #13616

Introduction to Bioassay & Bio-analytics From Pre-Clinical to Clinical trials

04/06/2013 #13213

Managing Calibration Systems as Part of the QA System

04/06/2013 #13132

Data Management & Statistical Methods in Clinical Trials

05/06/2013 #13269

Troubleshooting in Sterilization & Microbiological Testing of MD

05/06/2013 #13629

Thermal Validation and Monitoring in GMP Environment

06/06/2013 #13620

Flow Cytometry

11/06/2013 #S13641

Optimizing Study Design and Protocol Development in Clinical Trials

12/06/2013 #13370

ISO 14155 (2011) Clinical Trials for Medical Device is here

12/06/2013 #13087

Advanced HPLC

17/06/2013 #13617

Quality Management Systems for APIs

17/06/2013 #13193

UV FILTERS FOR HUMAN - CHEMISTRY, APPLICATIONS AND REGULATORY ASPECTS

17/06/2013 #13636

Physical Properties Characterization of Pharmaceutical Powders

17/06/2013 #P13721

רגולציה ו-GMP בתעשיית התרפיה התאית

18/06/2013 #13637

Good Weighing Procedures

19/06/2013 #13058

Fermentation

19/06/2013 #13492

נשאים לגידול ולהשתלה של תאים ותאי גזע

19/06/2013 #13038

Validation of Ethylene Oxide (EtO) Sterilisation

23/06/2013 #13625

Fungal Identification

24/06/2013 #13626

Disinfectant Qualification & Cleaning Procedures

24/06/2013 #13640

עדכוני GDP - GOOD DISTRIBUTION PRACTICE

24/06/2013 #13305

Regulatory and Quality requirements for the registration of Biologics/Biotechnology Products

01/07/2013 #13310

Water Systems in the Pharmaceutical & Biotechnological Industries

01/07/2013 #13458

ניהול וביצוע יעילים של חקירות-כשל בתהליכי הייצור הפרמצבטי

02/07/2013 #13638

Implementation of Worst Case Approach In Cleaning Validation Systems

02/07/2013 #13142

Method Development in GC-MS

03/07/2013 #13463

בקרת תיעוד

03/07/2013 #13077

Basics in Analytical Chemistry

03/07/2013 #13091

Advanced GC

07/07/2013 #13066B

CRA – Monitoring and Coordinating Clinical Trials

07/07/2013 #13069B

GCP - Good Clinical Practice

08/07/2013 #B13464

Drug Delivery Systems (DDS) Skin Delivery - From Pathways to Skin Penetration through Barrier Manipulation

08/07/2013 #13065

GLP

10/07/2013 #13163

Environmental Monitoring

10/07/2013 #13627

Skin Toxicology and Safety Assessment for Pharmaceutics, Cosmetics and Personal Care

10/07/2013 #13630

דרישות רגולטוריות בתחום האמ"ר (Medical Device), ישראל, אירופה (CE) EMA וארה"ב FDA, יום עיון למתחילים

17/07/2013 #13306

The European QP - Role, Responsibilities and Activities

22/07/2013 #13451

Pharmacovigilance Under Inspection How to Survive a Drug Safety Inspection

23/07/2013 #13452

Pharmacovigilance – Risk Management in Drug Safety Closing the Gap between the US and Europe

24/07/2013 #13438

Conducting Effective Pharmaceutical Compliance Audits

29/07/2013 #13618

ICH Quality Guidelines Q1- Q6 Product Development and Life Cycle

29/07/2013 #13635

PAT, NIR and QBD Advanced Course

05/08/2013 #13156

Good Engineering and Maintenance Practiceas a Critical Element of the Quality System

06/08/2013 #13244

Impurities in Active Pharmaceutical Ingredients (APIs) and in Pharmaceutical Products Impurities in Active Pharmaceutical Ingredients (APIs) and in Pharmaceutical Products

08/08/2013 #13034

R&D in a GMP Environment

10/09/2013 #13032

Supplier Approval – Managing Risks in Your Supply Chain

07/10/2013 #13151

Analytical Chemistry in the Pharmaceutical Raw Material Laboratory

09/10/2013 #13474

Application OF ICP-AES Inductively Coupled Plasma Atomic Emission & ICP-MS Mass Spectrometry

14/10/2013 #13466

איכות במעבדות QC

14/10/2013 #13099

Near Infra Red - NIR Spectroscopy

14/10/2013 #13427

יבוא מוצרים עפ"י חוק התקנים

16/10/2013 #13473

המוצר שלכם אינו מתאים לבית החולים האמריקאי...

16/10/2013 #13157

System & Equipment Qualification & Validation Including case-studies, handling deviations (+ a sneak peep at the FDA Process Validation Draft)

21/10/2013 #13173

Quality Assurance of Computerized Systems- A Comprehensive Perception

22/10/2013 #13639S

MDDMI Conference

28/10/2013 #13079

Process Analytical Technology – PAT (Beginners)

28/10/2013 #13619

SOP Review as a Tool for Continued Improvement

28/10/2013 #13432

Regulation of Combination Products

03/11/2013 #13069C

GCP - Good Clinical Practice

03/11/2013 #13066C

CRA – Monitoring and Coordinating Clinical Trials

04/11/2013 #13386

GAMP5 - יישום גישת ניהול סיכונים במערכות ממוחשבות

04/11/2013 #13086

Troubleshooting and Solving Problems in HPLC - Advanced Especially the experienced chemists might find be surprised

14/11/2013 #13169

Writing SOPs - Workshop To review the purpose of SOPs and to provide participants with tools to write their own SOPs that are clear, concise and not open to interpretation....

19/11/2013 #13043

Validation of Analytical Methods

19/11/2013 #13046

Quality assurance on calibration and measurements including the updated requirements according to the new edition of the ISO/IEC/EN17025 standard

26/11/2013 #13243

ICH, EMEA and FDA Guidelines for Drug and Drug-Substances Stability

03/12/2013 #13301

How Current Are You? Review of New Industry and Regulatory Expectations For Biopharmaceutical Products

03/12/2013 #13053

Regulatory Affairs of Medical Devices

09/12/2013 #13096

Atomic Absorption – AA

10/12/2013 #13078

Introduction to Chromatography

11/12/2013 #13036

GMPs for Printed Packaging Materials

15/12/2013 #13614

Solid Dosage Form Development – a QbD Approach

16/12/2013 #13247

Registration in Israel - Drugs, Biologics, Medical Devices and Cosmetics

18/12/2013 #13312

Formulation for Chemists

22/12/2013 #13274

Professional Retraining for Engineers: Join the Medical Device Industry

23/12/2013 #13095

Introduction to Mass Spectroscopy

26/12/2013 #13048

RA Managers in the Biomed Industry

29/12/2013 #13014

CQA – Developing Clinical Quality Assurance Audit Skills and Procedures

29/12/2013 #13281

Drug Safety Evaluation during Drug Development and Non-Clinical Studies This course provides a comprehensive explanation of the non-clinical development of drugs, biologics and combination products, emphasizing the princ...

30/12/2013 #13299

Process Scale-Up - Advanced Level

30/12/2013 #13185

Patient Recruitment Strategy: A Comprehensive Workshop for Investigative Sites and Sponsors The course focuses on the skills of the people who are responsible for recruitment success including their personal development (Me), their relation...

30/12/2013 #13253

Capsule Technology & Encapsulation of Commercial & Clinical Supplies A comprehensive capsule technology presentation covering the manufacturing of empty and filled two piece capsules, fundamentals of encapsulation, bl...

30/12/2013 #13256

Identification of Endogenous Compounds and Natural Products using LC–MS–MS Technologies

30/12/2013 #13257

Identification of Drug Metabolites using LC–MS–MS Technologies

30/12/2013 #13017

Biocompatibility Evaluation of Medical Devices & Biomaterials

30/12/2013 #13029

Introduction to GMP and Quality Assurance for Manufacture and Control of Finished Pharmaceuticals Participants will graduate this course with an understanding of the GMP regulations and an idea of how and why they need to be implemented

30/12/2013 #13215

Retrieving Compound Identity Using LC-MS-MS This two-day course provides knowledge for structure elucidation of small molecules (drugs, pesticides, natural products, etc.) by combined liquid c...

31/12/2013 #13275

Professional Qualification of R&D Personnel for the Generic Drug Industries

31/12/2013 #13337

Analytical Biotechnology: Method Development & Validation

31/12/2013 #13081

Sample Preparation in GC

31/12/2013 #13328

Color Testing

31/12/2013 #13186

Supply Chain Risk Management – an Interactive Workshop

31/12/2013 #13236

CRF Design Workshop

31/12/2013 #13088

Quantitation in Chromatography

31/12/2013 #13477

Optimizing Clinical Trials During Early Development Novel QBD Clinical Drug Development

31/12/2013 #13184

Listen to the Voice of Process - Control charts for use in establishing manufacturing processes stability

31/12/2013 #13102

Ion Chromatography

31/12/2013 #13124

Post-Marketing Strategies for Medical Devices – how to keep your device on the market

31/12/2013 #13271

Semi-Preparative Chromatography

31/12/2013 #13255

How to Prepare for a CMDCAS Audit This seminar is dedicated to manufacturers, who already have a quality management system according to ISO 13485, but who want to integrate the addit...

31/12/2013 #13273

Introduction to production of solid dosage forms

31/12/2013 #13080

Sample Preparation - Introduction

31/12/2013 #13149

HPLC Laboratory

31/12/2013 #13108

The New European Directive for Medical Devices This seminar focuses on the changes to the MDD (Directive 93/42/EEC) introduced by Directive 2007/47/EC and on the implementation guidance by NBOG.

31/12/2013 #13050

Introduction to Solid-State NMR and its Applications for the Pharmaceutical Industry

31/12/2013 #13055

Common Statistical Errors in Biological Experiments There are several pitfalls in the design, conduct and analysis of biological experiments. These are the source of some common errors that may seriou...

31/12/2013 #13376

Simulation/Mock FDA meeting Preparation

31/12/2013 #13020

Ethical Drug Development – From Research Product to Prescription Drug

31/12/2013 #13051

Film Coating Meeting the Needs of the Global Pharmaceutical Industry in the 21st Century

31/12/2013 #13011

Medical Devices: Validation and Documentation of Sterilization

31/12/2013 #13012

How to Identify and Manage Risks

31/12/2013 #13100

Modern Thin Layer Chromatography

31/12/2013 #13214

Quantitative Analysis by LC–MS One of the most important applications of LC–MS is its use in routine quantitative analysis, in preclinical and clinical studies to sustain drug dev...

31/12/2013 #13282

Preparing Protocols & Final Reports for Clinical Trial

31/12/2013 #13297

Gel Isoelectric Focusing (IEF) for the Characterization of Proteins and Peptides

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