Analytical Methods Validation for FDA Compliance
Sep 13 2010, Burlingame, CA |
CMC Submissions in CTD Format
Sep 20 2010, Burlingame, CA |
Sensory Evaluation
Sep 20 2010, New Brunswick, NJ |
Skin Product Development
Sep 20 2010, New Brunswick, NJ |
Documentation Management and Control
Sep 27 2010, East Brunswick, NJ |
Ingredients for Cosmetics and Toiletries
Sep 27 2010, East Brunswick, NJ |
Preparation, Packaging and Labeling of Clinical Trial Materials
Sep 27 2010, East Brunswick, NJ |
Preparing for and Surviving an FDA Inspection
Sep 29 2010, East Brunswick, NJ |
Generic Drug Approvals
Oct 04 2010, New Brunswick, NJ |
Introduction to Petroleum Refinery Processing
Oct 04 2010, Amsterdam, The Netherlands |
Patent Law
Oct 07 2010, East Brunswick, NJ |
Patent Law
Oct 07 2010, East Brunswick, NJ |
Skin Product Development
Oct 11 2010, Amsterdam, The Netherlands |
Lyophilization Technology
Oct 12 2010, New Brunswick, NJ |
Sulfonation and Sulfation Technology
Oct 13 2010, New Brunswick, NJ |
Design Control and Product Validation
Oct 18 2010, New Brunswick, NJ |
Powders: Their Properties and Processing
Oct 18 2010, Amsterdam, The Netherlands |
Preparation, Packaging and Labeling of Clinical Trial Materials
Oct 18 2010, Amsterdam, The Netherlands |
Developing and Maintaining an Effective Complaint System
Oct 20 2010, New Brunswick, NJ |
Developing and Maintaining an Effective Complaint System
Oct 20 2010, New Brunswick, NJ |
Developing and Maintaining an Effective Complaint System
Oct 20 2010, New Brunswick, NJ |
Analytical Methods Validation for FDA Compliance
Oct 25 2010, Amsterdam, The Netherlands |
Conducting Effective Quality Audits
Oct 25 2010, New Brunswick, NJ |
Surfactants, Colloids and Interfaces
Oct 26 2010, New Brunswick, NJ |
Pharmaceutical Supervisory Management Skills
Oct 27 2010, East Brunswick, NJ |
Mixing of Liquids and Complex Materials
Nov 01 2010, New Brunswick, NJ |
Gums and Hydrocolloids
Nov 02 2010, New Brunswick, NJ |
Root Cause Investigation for CAPA
Nov 02 2010, New Brunswick, NJ |
CMC Submissions in CTD Format
Nov 04 2010, Amsterdam, The Netherlands |
Microbiological Control and Validation
Nov 08 2010, Amsterdam, The Netherlands |
Piping Design, Analysis and Fabrication
Nov 08 2010, Amsterdam, The Netherlands |
Fired Process Heaters
Nov 15 2010, Amsterdam, The Netherlands |
Critical Process Cleaning and Cleaning Validation
Dec 01 2010, Amsterdam, The Netherlands |
Transdermal Drug Delivery
Dec 02 2010, New Brunswick, NJ |
Drug Product Stability and Shelf-Life
Dec 13 2010, Amsterdam, The Netherlands |
ICH-Q7
Dec 13 2010, Amsterdam, The Netherlands |
ICH-Q7
Dec 13 2010, Amsterdam, The Netherlands |
Strategies for 21 CFR Part 11 Cost Effective Compliance Using a Risk-based Approach
2225 |
A Survey of Microbiology for the Pharmaceutical, Biotechnology, and Medical Device Industries
2317 |
Active Pharmaceutical Ingredients
840 |
Active Pharmaceutical Ingredients
840 |
ADME Fundamentals
2077 |
Advanced Tablet Press Operation
2206 |
Aerosol Technology
669 |
An Introduction to Food Manufacturing Operations
2364 |
An Introduction to Pathways for Skin Penetration
2403 |
An Overview of Documentation Requirements in FDA Regulated Industries
2325 |
An Overview of Process Validation for the Pharmaceutical, Medical Device and Related Industries
2303 |
Annual Product Reviews (APRs) For Pharmaceuticals
1998 |
Annual Product Reviews (APRs) For Pharmaceuticals
1998 |
Antiperspirants and Deodorant Technology: Principles and Applications
1915 |
Applied cGMPs for Pharmaceutical and Allied Industries
610 |
Assuring Quality of Supplies to Pharmaceutical and Related Industries
2387 |
Assuring Your Supply Chain through Supplier Qualification
2227 |
Atomization, Sprays and Atomizers
1883 |
Auditing and Inspecting Preclinical Research for GLP Compliance
1774 |
Auditing for cGMP Compliance
1881 |
Best Practices in SAS Statistical Programming for Regulatory Submission
2234 |
Best Practices in SAS Statistical Programming for Regulatory Submission
2234 |
Best Practices in SAS Statistical Programming for Regulatory Submission: Creating Publication-Quality Summary Tables (SECOND in a Two-Part Series)
2214 |
Best Practices in SAS Statistical Programming for Regulatory Submission: Understanding and Applying the QC Plan to Validate Summary Tables (FIRST in a Two-Part Series)
2213 |
Biocidal and Plant Protection Products in the EU: Borderlines and Overlaps
2218 |
Biopharmaceutical Process Systems
1116 |
Biosafety of Biological Drug Products
2228 |
Bringing Nanotechnology to Your Market
2157 |
Calibration in the FDA Regulated Industry
2026 |
CAPA - The Heart of Your Quality System
2124 |
CAPA - The Heart of Your Quality System
2124 |
Catch the Wind–Current and Future Utilization of Wind Power
2353 |
CDRH: Get Ready for Changes!
2405 |
cGMP Auditing - Strategies for Compliance
2012 |
cGMP for Pharmaceutical Production Supervisors
604 |
cGTP in a Nutshell
2179 |
cGTP in a Nutshell
2179 |
Choosing Sensors, Monitors and Instruments for PAT Programs
2128 |
Claim Substantiation for Clinical Studies of Cosmetic Products
2370 |
Clean Coal Technology: A Clear Picture
2331 |
Clean Room Technology
23 |
Clean Room Technology Basics in a Nutshell (First in a Three Part Series)
2420 |
Meeting Today’s FDA Requirements for Clinical Trial Processes
2271 |
Clinical Testing Submissions
2272 |
Coextrusion Technology
1613 |
Color Additive Basics for Decorative Cosmetics
2186 |
Color Additives and Their Use in Decorative Cosmetics
2114 |
Color Selection for Decorative Cosmetics
2182 |
Combination Product Development: Safety/Registration/Approval
2104 |
Combination Products: How to Approach the Proposed Manufacturing and Distribution Requirements
2392 |
Commissioning, Qualification and Validation
1954 |
Complaint Systems - The Essential Requirements
2132 |
Complaint Systems - The Essential Requirements
2132 |
Computerized Systems Used in Clinical Investigations: the New FDA Guidance
2184 |
Conception, Design and Implementation of Plant Safety Systems
1672 |
Conducting Compliant Endotoxin Testing
2185 |
Control of Microbial Contamination in Manufacture of Sterile and Non-Sterile Products
2215 |
Corrosion Control in Industry and Plants
446 |
Corrosion Control in the Oil and Gas Industry
1198 |
Corrosion Control in the Oil and Gas Industry
1198 |
Cosmeceutical Products, Market and Claims
2256 |
Cosmetic Colorant Global Market, Regulations and Trends
2288 |
Cosmetic Product Formulation
1350 |
Cost Effective Quality-by-Design and Critical-to-Quality Tools for PAT
2127 |
Cost Effective Quality-by-Design and Critical-to-Quality Tools for PAT
2127 |
Crackdown on Institutional Review Boards (IRBs)
2334 |
Creating Fragrance for a Green World
2238 |
Critical Limits, Monitoring and Corrective Actions–A HACCP Review
2285 |
Crystallization Technology
149 |
CSOs: Are They Right for You?
2240 |
Current Applications and Future Potential of Biofuels
2328 |
Current EU Chemical Control Regulations, from REACH to the GHS–EU Focus
2291 |
Current Good Manufacturing Practice (cGMP) for Purchasing
1836 |
Current Good Tissue Practices (cGTPs)
2086 |
Current Rules, Guidance Documents and Implementation Status for REACH–Fall 2009
2341 |
Data Integrity: The Proof’s in the Inputting
2343 |
Decorative Cosmetics–Using Absorption and Pearl Pigments
2183 |
Delivery Systems in Personal Care
2402 |
Developing Specifications for Drug Substances (APIs) and Drug Products
1918 |
Distillation
513 |
DQ: A Guide to Protecting Your Interests When Procuring Sensors
2200 |
Developing Specifications for Drug Substances (APIs) and Drug Products
1918 |
Developing Specifications for Drug Substances (APIs) and Drug Products
1918 |
Dry Food Manufacturing Operations
2369 |
Early Stage Clinical Studies for Drugs and Devices
2118 |
Effective Clinical Data Acceptance Testing
2250 |
Effective Project Management
129 |
Effective Tools in Selecting a CRO
2296 |
Effectively Managing CROs
2298 |
Effects of Psychological Factors and Stress on Skin Inflammatory Disorders
2282 |
Efficient Nozzle Atomization
2417 |
Efficient Wheel and Two-Fluid Atomization
2419 |
Elements of Applied Process Engineering
1512 |
Suspensions and Emulsions in Pharmaceuticals and Food
274 |
Encapsulation: Basic Techniques and Applications
2196 |
Endotoxin Testing: Drugs, Medical Devices and Biopharmaceuticals
526 |
Endotoxin Testing: Resolving Interference and Test Validation
2204 |
Environmental Control and Monitoring
1937 |
Environmental Monitoring for Non-Sterile Drugs
2397 |
Equipment Qualification in a Nutshell
2135 |
Equipment Qualification in a Nutshell
2135 |
Everything You Wanted to Know About Antiperspirants in 90 Minutes
2190 |
Evolution of the Pharmaceutical Industry through 2020
2198 |
Excipient GMPs
2050 |
Failure to Warn and Medical Device Preemption
2316 |
Failure to Warn and Preemption
2315 |
FDA Drug Development and Compliance
587 |
FDA Quarterly Briefing–July 2008
2230 |
FDA Quarterly Briefing: Focus on Biotechnology February, 2010
2371 |
FDA Quarterly Briefing: Focus on Medical Device News–December, 2009
2358 |
FDA Quarterly Briefing: Focus on Medical Device News–March 2010
2375 |
FDA Quarterly Briefing: Focus on Pharmaceuticals – January 2010
2360 |
FDA Quarterly Briefing–April 2009
2233 |
FDA Quarterly Briefing–January 2009
2232 |
FDA Quarterly Briefing–July 2009
2267 |
FDA Quarterly Briefing–October 2008
2231 |
FDA Quarterly Briefing–October 2009
2268 |
FDA Quarterly Update–July 2010
2415 |
FDA Quarterly Update–July 2010
2415 |
FDA to Regulate Tobacco: What to Expect
2330 |
Filtration One: The Process, The Equipment, The Equations
2422 |
Filtration Two: Expression, Media, Pretreatment, Operating Tips
2424 |
Flavors -- Their Creation, Definition and Use
246 |
Fluid Flow and Line Sizing
2162 |
Food Extrusion Technology
689 |
Food Manufacturing Layout and Design
2365 |
Food Safety and Regulations
2366 |
Food Supplements, Additives and Herbal Medicines
2257 |
Food Traceability: Delivering High Quality and Safe Products to the Consumer
2342 |
Fragrance and the Mind
2254 |
Fragrance for the Chemist
2253 |
From Functional Siloxanes to Performance Enhancing Applications
2262 |
Fundamentals of Biochemistry: Background for Biotechnology
33 |
Fundamentals of Biotechnology
2197 |
Fundamentals of Molecular Biology and Genetic Engineering
1377 |
Fundamentals of Nanotechnology
2111 |
Gasification Technology
1997 |
Getting a Share of the BioDefense Grant Billions
2205 |
Global Cosmetic Regulations: Going Green
2226 |
Globally Harmonized Systems (GHS)
2201 |
GMP for Dietary Supplements
2094 |
Good Clinical Practices (GCP)
107 |
Good Distribution Practices
2116 |
Good Laboratory Practices (GLP)
545 |
Granulation, Tabletting and Capsule Technology
541 |
Greening of Global Cosmetic Regulations
2222 |
Guidelines for Skin Absorption Studies
2220 |
Guidelines to In Vitro Skin Absorption Studies
2202 |
HACCP: Critical Limits, Monitoring and Corrective Actions – An Introduction and Review (Second in a Three Part Series)
2167 |
HACCP: Hazard Analysis and Critical Control Points – An Introduction and Review (First in a Three Part Series)
2166 |
HACCP: Verification and Record Keeping – An Introduction and Review (Third in a Three Part Series)
2168 |
Hair Product Development
2076 |
Heat Exchanger Design in an Energy Conscious World
2348 |
Heat Exchangers: Equipment, Design and Operation
2180 |
History, Theory, and Instrumentation of Near-Infrared Spectroscopy
2318 |
Hydrogenation Technology
150 |
ICH Q10: Pharmaceutical Quality System
2131 |
Pharmaceutical Risk Management Tools: Getting the Most Out of ICH Q9
2158 |
Implementing and Managing the Medical Device Complaint System
2339 |
Implementing GEP (Good Engineering Practices) in the Pharmaceutical, Bio-Pharmaceutical, and Medical Device Industries
2284 |
Improving Drug Delivery Through the Use of Polymers
2382 |
Safety Assessment of Cosmetic Ingredients and Formulations
2161 |
Safety Assessment of Cosmetic Ingredients and Formulations
2161 |
INDs/NDAs/CTDs
448 |
INDs/NDAs/CTDs
448 |
Industrial Drying of Heat Sensitive Materials
767 |
Industrial Ink Technology
1579 |
Industrial Membrane Separations
677 |
Industrial Rheology
1025 |
Initiatives in the Cosmetic and Personal Care Industry
2299 |
Initiatives in the Cosmetic and Personal Care Industry
2299 |
Instrumental Methods for Pharmaceutical Trace Metals Analysis
2321 |
International Patent Law
2100 |
International Patent Law
2100 |
International Regulatory Update for the Personal Care Products Industry: Focus on the European Union, Latin America & Canada
2301 |
Introduction to cGMP System-Based Audits
2309 |
Introduction to Drug Delivery Technology
2084 |
Introduction to Natural Gas Processing
1605 |
Introduction To Pharmaceutical cGMP
2244 |
Introduction to Skin Aging
2125 |
Introduction to Skin Aging
2125 |
Investigation of Microbial Contamination in Sterile and Non-Sterile Products
2216 |
IQ, OQ, PQ
1808 |
ISO 13485, ISO 9001 and QSR Regulations for Medical Device Companies
2092 |
It's Not Easy Going Green: Preparing for the Greening of Cosmetic Regulations
2336 |
Key PAT and QbD Concepts: Quality Systems Integration Strategies (QSIS)
2322 |
Key PAT Concepts: Focus on Design of Experiment
2304 |
Key PAT Concepts: Focus on Design Space
2289 |
Key PAT Concepts: Focus on Desired State
2305 |
Keys to Risk Management: Implementation, Documentation, Monitoring and Mitigation
2332 |
Laboratory Control System
2047 |
Laboratory Control System
2047 |
Endotoxin Testing: Drugs, Medical Devices and Biopharmaceuticals
526 |
Lean Methodology: Eliminate Waste, Improve Efficiency, Increase Profits
2345 |
Lyophilization 101: Principles, Physical Properties and Characterization Techniques
2236 |
Lyophilization 101: Scale-Up, Cycle Transfer, and Sonic Water Vapor Flow
2263 |
Lyophilization: Optimized Pre-Formulation, Formulation, and Cycle Development Techniques
2241 |
Machinery Failure Analysis and Prevention (US Course)
1054 |
Machinery Failure Analysis and Prevention (European Course)
2235 |
Machinery Failure Analysis and Prevention (US Course)
1054 |
Malodor–Production and Prevention
2404 |
Managing Multiple Projects in a Resource Limited Environment
1114 |
Managing Multiple Projects Utilizing Lean Manufacturing Techniques
2261 |
Measurement Uncertainty in Analytical Chemistry
2401 |
Medical Device Regulatory Compliance
1992 |
Meeting Today’s FDA Requirements for Clinical Trial Processes
2271 |
Microbial Challenge and Shelf Life Testing for Foods
2283 |
Microbial Challenge Testing for Foods
2273 |
Microbial Shelf Life and Challenge Testing for Foods (Second in a Three-Part Series)
2209 |
Microbiological Quality of Water-Based Consumer Products
1383 |
Microbiology Fundamentals Relating to Clean Rooms (Second in a Three Part Series)
2426 |
Microencapsulation and Particle Coating
774 |
Natural Ingredients in Formulating Skin Care Products
2239 |
Near Infrared Spectroscopy
1583 |
Near Infrared Spectroscopy
1583 |
Non-Clinical Drug Safety Evaluation and Drug Development
1153 |
Nutritional Supplement Formulation Basics
2246 |
Operation of the Clean Room (Third in a Three Part Series)
2427 |
Optimizing Energy Use in Nuisance Dust Collection Applications
2399 |
Orphan Drug Application and Submission
2223 |
Overcoming the Challenges to Transdermal Drug Delivery Development–An Introduction
2383 |
Packaging of Pharmaceuticals
42 |
PAI: Surviving the Pre-Approval Inspection
2396 |
Particle Size Reduction I: General Aspects, Physics of Breakage, Shape, Size and Surface (First in a two-part series)
2429 |
Particle Size Reduction II: Size Reduction Equipment, Equipment Operation, Energy Requirements (Second in a two-part series)
2430 |
PAT Online Process Analysis
2030 |
PAT-Based Downstream Protein Purification
2130 |
Pathways to Skin Penetration
2149 |
Economics of Petroleum Refining
2134 |
Pharma: Concept To Consumer
2115 |
Pharmaceutical cGMP-Quality Systems
2245 |
Applied cGMPs for Pharmaceutical and Allied Industries
610 |
Pharmaceutical Process Development
1358 |
Pharmaceutical Process Validation Basics
2327 |
Pharmaceutical Quality Assurance and Control
224 |
Pharmaceutical Risk Management Tools: Getting the Most Out of ICH Q9
2158 |
Pharmaceutical Technology Transfer
2095 |
Near Infrared Spectroscopy
1583 |
Pharmaceutical Water and the International Regulatory Environment
2212 |
Pharmaceutical Water Sampling and Testing
2259 |
Pharmaceutical Water System–Design and Operation
2258 |
Pharmaceutical Water Systems
1802 |
Pharmaceutical Water Systems: Validation and Start-Up
2260 |
Pharmaceutical Water: Chemistry, System Design and Validation
2211 |
Pilot Plant and Scale-up Studies
1882 |
Pneumatic Conveying for Bulk Solids
727 |
Polymers and Their Use in the Medical Device Industry
2293 |
Powder Mixing Technology
777 |
Practical Steps to Understanding ICH Q9
2160 |
Preparing for the Device Industry's 513 Exemption Changes
2408 |
Preparing for the International Harmonization of Medical Devices
2381 |
Preservatives and Antimicrobials in Cosmetic, Food and Personal Care Products
2255 |
Preservatives and Biocides in Consumer Products
2221 |
Real World Approaches to PAT and QbD Implementation
2085 |
Real World Approaches to PAT and QbD Implementation
2085 |
Real World Approaches to PAT and QbD Implementation
2085 |
Process Plant Start-Up
561 |
Process Validation for Packaging of Pharmaceuticals and Medical Devices
1789 |
Process Validation for the Pharmaceutical and Medical Device Industries
736 |
Process Validation for the Pharmaceutical and Medical Device Industries
736 |
Protecting the Food Supply from Terrorists: What the Food Industry Needs to Know
2237 |
Qualification and Validation of Analytical Methods for Protein Products
1933 |
Quality Control and Flavor Usage in Foods
2300 |
Radiation Curing: Ultraviolet Light and Electron Beam Technology
592 |
REACH Alert: Current Rules, Guidance Documents and Implementation Status
2286 |
REACH: Registration, Evaluation and Authorization of Chemicals
2145 |
Real World Approaches to PAT and QbD Implementation
2085 |
Recognizing and Preventing Data Integrity Issues
2349 |
Recovering Energy from Flowing Water– Hydroelectric, Tidal and Wave Technologies
2355 |
Recovering Energy from the Earth– Geothermal and Oceanic Processes
2354 |
Refractories for Industrial Applications
551 |
Refrigerated and Frozen Food Operations
2368 |
Regulatory Compliance for the Personal Care Products Industry
1522 |
Risk Management Today: Complying with the ISO 14971: 2007 Standard
2106 |
Risk Management Today: Complying with the ISO 14971: 2007 Standard
2106 |
Risk Hazard Assessment for Validation– ISO14971, HACCP, FMEA, FAULT TREE
2147 |
Risk Hazard Assessment for Validation– ISO14971, HACCP, FMEA, FAULT TREE
2147 |
Risk Management in a Nutshell
2156 |
Risk Management Today: Complying with the ISO 14971: 2007 Standard
2106 |
Role of PAT and QbD in Biologic Drug Production
2163 |
Role of Pharmaceutical QA/QC in Quality Systems
2294 |
Safety Assessment of Cosmetic Ingredients and Formulations
2161 |
Scale-Up and Post Approval Changes Guidelines (SUPAC & API Changes)
1948 |
Scale-Up and Post Approval Changes Guidelines (SUPAC & API Changes)
1948 |
Commissioning, Qualification and Validation
1954 |
Selecting and Managing CROs
2032 |
Selecting a Drug Product Candidate Using Quality Risk Management: PAT & QbD
2126 |
Selecting a Drug Product Candidate Using Quality Risk Management: PAT & QbD
2126 |
Silicon to Siloxanes: Chemistry and Properties
2247 |
Siloxane Technology and Personal Care Applications
2207 |
Skin Inflammation – Reasons, Prevention, Treatment and Testing
2217 |
Skin Inflammation: From Triggers to Aging
2274 |
Solar Energy–Capturing and Utilizing Sunlight
2352 |
Starch: Chemistry, Properties and Applications
542 |
Sterile Products: Formulation, Manufacture and Quality Assurance
435 |
Sterile Products: Formulation, Manufacture and Quality Assurance
435 |
Sterilization in the Pharmaceutical Industry
2075 |
Strategies for 21 CFR Part 11 Cost Effective Compliance Using a Risk-based Approach
2225 |
Strategies for Leveraging PAT/QbD in Biologic Applications
2287 |
Sunlight Exposure to the Skin: Can We Shield the Bad and Enhance the Good?
2410 |
Sunscreen Regulation Technology and Product Development
2017 |
Sunscreen Regulation Technology and Product Development
2017 |
Sunscreens 360°: Regulatory Overview and Update
2302 |
Sunscreens: Global Marketing and Product Trends
2165 |
Sunscreens: Global Marketing and Product Trends
2165 |
Surviving an FDA Inspection -- FDA Inspections of Non-U.S. Sites
1880 |
Suspensions and Emulsions in Pharmaceuticals and Food
274 |
System Validation, GAMP Harmonization and P.A.T
913 |
System Validation, GAMP Harmonization and P.A.T
2203 |
Systems Approach to Sustainable Energy Solutions
2356 |
Tablet Production for Operators and Supervisors
1428 |
Tactics to an Effective FDA Submission
2379 |
Taking the Mystique out of Silicones for the Personal Care Industry
2195 |
Technical Writing in the Pharmaceutical and Allied Industries
162 |
Technical Writing in the Pharmaceutical and Allied Industries
162 |
Testing for Acute Chemical Toxicity – In Vitro Approaches Compliance with REACH and the 7th Amendment
2323 |
Testing for Cytotoxicity-Compliance with REACH and the 7th Amendment
2278 |
Testing for Eye Irritation and Corrosion: Compliance with REACH and the 7th Amendment
2276 |
Testing for Genotoxicity, Mutagenicity and Carcinogenicity: Compliance with REACH and the 7th Amendment
2280 |
Testing for Photo-Toxicity: Compliance with REACH and the 7th Amendment
2277 |
Testing for Skin Irritation, Corrosion and Sensitization: Compliance with REACH and the 7th Amendment
2269 |
Testing for Toxicity to Reproduction and Endocrine Disruption – Compliance with REACH and the 7th Amendment
2279 |
The China Syndrome: Quality Issues in Manufacturing
2337 |
The Coming Medical Device Revolution
2338 |
The Do’s, Don’ts, and Whys of HPLC
2400 |
The Generation of Wrinkles-Biochemistry and Prevention
2411 |
GLP Study Director
2136 |
The International Cosmetic Ingredient Dictionary and Handbook: The Process and Impact for Back Label Disclosure
2170 |
Quality System
2046 |
Thermal Process Operations
2367 |
Topical Antiseptic Product Development
2219 |
Toxicokinetics and Skin Metabolism Testing: Compliance with REACH and the 7th Amendment
2281 |
FDA Drug Development and Compliance
587 |
FDA Drug Development and Compliance
587 |
Understanding and Using Microbial Computer Modeling in Food Microbiology (Third in a Three-Part Series)
2210 |
Understanding and Using Microbial Sampling Plans for Foods (First in a Three-Part Series)
2208 |
Understanding Juice Production: Raw Material, Processes, Packaging and Issues
2409 |
Understanding Pharma: Business Growth and Drivers
2199 |
Current Applications and Future Potential of Biofuels
2328 |
Updates on Process Validation for Medical Devices…New Approaches and Practice
2394 |
USP Guidelines for Product Quality and Product Performance Tests
2326 |
Vendor and Contract Supplier Qualification
1984 |
Waste Incineration and the Combustion Process
71 |
Bringing Nanotechnology to Your Market
2157 |
What is the Pharma Quality System and Why Should I Care?
2418 |
Who REALLY Regulates Your Pizza and Is It COOL?
2320 |
Writing and Implementing Clinical Protocols
772 |
Writing SOPs for cGMP Compliance
1646 |