Good Laboratory Practices (GLP)

The main intent of this course is to review the requirements imposed by Good Laboratory Practices (GLP) regulations for facilities engaged in toxicology and product safety testing, primarily in animals and biological test systems. The responsibilities and functions of management including the Study Director, Principal Investigator and the Quality Assurance Unit (QAU) will be covered. Various procedures for meeting the requirements of the regulations will be presented. The lectures will be s...
CfPA

Current Concepts in Cardiopulmonary Care - Austin

This two-day course is geared to providing the new and experienced nurse, CRNA and respiratory therapist with a review of cardiopulmonary system pathophysiology along with common issues seen often in today’s environment. Also a review of heart failure, along with pulmonary hypertension, will be presented with common treatment plans. Finally, a discussion and presentation of sepsis and its effects on the heart and lungs will also be presented. PROGRAM LEARNING OUTCOMES This program prepa...
MED-ED

Four Key Elements of Moisturization

Who Should Attend? This course will be especially beneficial for Formulators, R&D Managers, Technicians, Sales & Marketing personnel in charge of skin care products and working with ingredients like moisturizers, humectant, and emollients actives Course Description Each year, hundreds of new ingredients with moisturizing claims are launched on the market. It is necessary to sort out and overcome the struggle of finding the right ingredients that will enable you to deliver as per consumer ...
CfPA

Crystallization Processes and Applications in Food Products

Who Should Attend? This training is especially designed for Chemists, Engineers, Scientists, Formulators, Managers, and Technicians involved in manufacture, formulation, and research and development of foods formulated through crystallization processes. Course Description This 90-minute accredited training course will cover the fundamental roles crystals and crystal microstructures play in the texture, appearance, mechanical properties, mouthfeel, shelf life and overall quality of many fo...
CfPA

Emulsions in the Beverage Industry

Who Should Attend? This online training will benefit professionals in the food and dietary supplement industries. It will be especially worthwhile to professionals with the following job functions in those industries: Engineers, Chemists, Scientists, Formulators, Managers, and Technicians involved in formulation, manufacturing, research and development and QC of beverages. Course Description This 90-minute, accredited training course offers a basic understanding of the behavior and pr...
CfPA

Softgel Capsules: Formulation Design and Troubleshooting

Who Should Attend? This broadly based course is intended for operators, troubleshooters and all scientists and technologists concerned with the development and processing of softgels capsules products and with related regulatory affairs. The material will be presented in such a way as to be of value to a varying level of expertise. This course will especially benefit those in: • Formulating • Manufacturing/Production • Engineering Support • R&D • Quality Assurance...
CfPA

Granulation, Tabletting and Capsule Technology

Who Should Attend? This broadly based course is intended for all scientists and technologists concerned with the development and processing of tablets, capsules and similar products, and with related drug regulatory affairs. The material will be presented in such a way as to be of value to a varying level of expertise. This course will especially benefit those in: • Quality Assurance • Marketing • Validation • Purchasing • R&D • Regulatory Affairs • Man...
CfPA

Charge Nurse Boot Camp - Pendleton

This course is geared toward new charge nurses or charge nurses that would like to kick their skills up a notch. Most charge nurses are promoted because of their clinical skills but are lacking in the other basic skills they need to lead in today’s shifting healthcare environment. This course will cover basics such as communication, conflict management, budgeting, relevant laws and other important concepts of leadership. Program Learning Outcomes This program prepares the learner to: ...
MED-ED

Responding to Golden Hour Emergencies: An Interactive, Case Scenario Approach - Daytona Beach

This course is designed for healthcare professionals who are caring for adult hospitalized patients with a time-sensitive emergency. Through the use of case scenarios, the focus is on the rapid assessment, triage and treatment of the three most time sensitive emergencies in hospitalized adults: acute coronary syndrome, stroke and sepsis. The program will address the process of moving the patient quickly through assessment, diagnosis and evidence-based treatment protocols, along with discussion...
MED-ED

Formulation Design and Troubleshooting of Pharmaceutical Dosage Forms: Tablets

Who Should Attend? This is an in depth course intended for product development scientists and technologists and support groups concerned with the development, designing and processing of tablets and similar oral products. The material will be presented in such a way as to be of value to a varying level of expertise. This course will especially benefit those in: • Formulation Development • Quality Assurance • Research and Development • Validation • Regulatory Affa...
CfPA

Drug Product Stability and Shelf-Life

Who Should Attend? This course contains in-depth coverage of the science and practice of drug stability, shelf-life and is designed to benefit the following personnel: • QC/QA Managers/Supervisors • Product Stability Managers • Manufacturing Personnel • Research & Product Development Scientists and Managers • Regulatory Personnel • Pharmaceutical Consultants Course Description This course focuses on the science and principles concerning stability of pharmac...
CfPA

Developing Specifications for Drug Substances and Drug Products

Who Should Attend? This course is intended for those who want to improve their understanding of the overall process of developing specifications for drug substance and drug products from generic, OTC and research-based pharmaceutical industries. The course includes both basic and advanced level topics of interest to: • Pharmacists • Analytical and Pharmaceutical Chemists • Staff from Chemical Production Departments • QA and QC Professionals • Regulatory Affairs Per...
CfPA

Early Drug Development

Who Should Attend? This course is intended for professionals who participate in, or are responsible for, drug development in small or large corporations in the pharmaceutical or biopharmaceutical industries. It is orientated particularly toward those with relatively limited development experience but offers benefit to all members or representatives on early-stage drug-development project teams and their managers, especially: • Non-clinical and clinical safety scientists • Pharmacok...
CfPA

Atomization and Spray Drying: Applied and Practical Approach

Who Should Attend? The course is intended for professionals working in the Food, Beverage,Specialty Chemical, Pharmaceutical, Pulp/Paper, and Pilot Plant industries. It will be especially valuable to: • Operations, Engineers, Scientists • Quality Control, Environmental, Health and Safety Professionals • Anyone involved with spray-dependent processes Course Description This 3-day accredited course focuses on Atomization and Spray-Drying technology, which are key processes in...
CfPA

GLP Study Director

Who Should Attend? This course is designed for those who already have some experience in managing GLP studies; those who wish to extend their role to study direction and their competence in study management, particularly in the complex multi-site environment. The course will benefit the following individuals: • Existing Study Directors who wish to upgrade their competence in a multi-site situation • The newly appointed Study Director • Study Supervisors who wish to bec...
CfPA

GLP and Quality Assurance: Developing a GLP Compliant QA Program

Who Should Attend? The participants in this course will already know the basics of GLP. The course is designed for those who wish to master how to implement and maintain a GLP QA function. The course explores quality issues within preclinical GLP and provides an opportunity for experienced personnel to update their competencies. Participants may come from: • Life-Science Industries • Academia • Government • Contract Testing Facilities Course Description This 2-day in...
CfPA

Good Laboratory Practices (GLP)

The main intent of this course is to review the requirements imposed by Good Laboratory Practices (GLP) regulations for facilities engaged in toxicology and product safety testing, primarily in animals and biological test systems. The responsibilities and functions of management including the Study Director, Principal Investigator and the Quality Assurance Unit (QAU) will be covered. Various procedures for meeting the requirements of the regulations will be presented. The lectures will be s...
CfPA

Everything Cardiac - Reno

This program provides a clinically applicable review of cardiovascular physiology and pathophysiology, cardiac assessment, cardiovascular pharmacology and interventions based on current guidelines for the most common cardiac disorders seen in clinical practice. Content includes a review of cardiac physiology that can be applied in daily practice, the physiological basis for cardiovascular drug therapy and the pathophysiology, diagnosis and guideline-based treatment strategies for heart failure...
MED-ED

Responding to Golden Hour Emergencies: An Interactive, Case Scenario Approach - Baltimore

This course is designed for healthcare professionals who are caring for adult hospitalized patients with a time-sensitive emergency. Through the use of case scenarios, the focus is on the rapid assessment, triage and treatment of the three most time sensitive emergencies in hospitalized adults: acute coronary syndrome, stroke and sepsis. The program will address the process of moving the patient quickly through assessment, diagnosis and evidence-based treatment protocols, along with discussion...
MED-ED

Critical Care Concepts: Beyond the Basics - Asheville

Although there are many programs available for those working in critical care, there is a need for those that are considered the "experts" to be challenged and further build their critical thinking skills. With the constant changes in evidence-based practice that drives what and why we do what we do, for many of us the only way to stay on top of the changes is through interaction in seminar format. Come learn, grow, and be challenged as we move beyond the basics with the sickest of our patient...
MED-ED

Everything Cardiac - Sacramento

This program provides a clinically applicable review of cardiovascular physiology and pathophysiology, cardiac assessment, cardiovascular pharmacology and interventions based on current guidelines for the most common cardiac disorders seen in clinical practice. Content includes a review of cardiac physiology that can be applied in daily practice, the physiological basis for cardiovascular drug therapy and the pathophysiology, diagnosis and guideline-based treatment strategies for heart failure...
MED-ED

Pharmaceutical Process Development

Who Should Attend? This course is intended for personnel in process development, technical service and pilot plant groups within the pharmaceutical industry. This includes personnel responsible for manufacturing of dosage forms for clinical studies. It will also be of value to personnel in: • Research & Development • Analytical Services • Product Development • Manufacturing • Production • Quality Assurance • Regulatory Affairs • CMC Projects Th...
CfPA

Protein Aggregation: Mechanisms, Particle Formation, Advanced Characterization & Rheology

Who Should Attend? This course will be of interest and value to scientists, formulators, supervisors, and managers engaged in development, production, analytical characterization and approval of biotherapeutics and who require a good working knowledge of protein aggregation. The training will be beneficial to those working in such areas as, • R&D • Protein Biochemistry/Biophysics • Quality Assurance/Quality Control • Stability • Formulation • Production T...
CfPA

How to Conduct Robust Root Cause Investigations for CAPA

Who Should Attend? This is an informative and interactive seminar for professionals in the pharmaceutical, biological, and medical device industries who conduct deviations, Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) investigations, especially for professionals in the following disciplines: • Quality Control Analysts • R&D • Quality Assurance • Manufacturing • Product/Process Development • Engineering Course Description One of t...
CfPA

Maternal Newborn Nursing Exam Review - Scottsdale

Presented in lecture format, this course reviews topics for the National Certification Corporation (NCC) examination “Maternal Newborn Nursing." Elements of the examination are discussed, followed by a review of the content. The major components include disease processes during pregnancy, maternal and fetal complications, postpartum and neonatal assessments. Practice questions are integrated throughout the presentation. PROGRAM LEARNING OUTCOMES This program prepares the learner to: 1...
MED-ED

Inpatient Obstetric Nursing Exam Review - Scottsdale

This course will assist nurses in reviewing the basic knowledge of biological, physiological, psychological and socio-cultural factors that influence the pregnant family, developing fetus and newborn. We will identify alterations in the status of the mother and the fetus and/or potential problems that could occur during the woman’s childbearing experience. We will evaluate interventions and plan of care for the complicated perinatal patient using the latest standards of care and current evid...
MED-ED

Formulation Design and Troubleshooting of Pharmaceutical Dosage Forms: Tablets

Who Should Attend? This is an in depth course intended for product development scientists and technologists and support groups concerned with the development, designing and processing of tablets and similar oral products. The material will be presented in such a way as to be of value to a varying level of expertise. This course will especially benefit those in: • Formulation Development • Quality Assurance • Research and Development • Validation • Regulatory Affa...
CfPA

Setting Up and Implementing Supplier Audits

Who Should Attend? This accredited training will be of value to those professionals in the pharmaceutical, medical device and related industries responsible for or involved in any interaction with suppliers, including those in the following functions: • Top Management • Audit • QA/QC • R&D • Manufacturing • Regulatory Affairs • Laboratories • Purchasing • Technical Services • Legal • Validation • Documentation Management Course De...
CfPA

Failure Analysis Basics for CAPA Systems

Who Should Attend? This 2-day course is intended for professionals from U.S. and international companies in the pharmaceutical, biologic, medical device and combination product industries and personnel who want to understand, manage, and utilize basic CAPA system concepts. The professionals who will benefit most from attending this course include: • Senior management • Regulatory Affairs, Regulatory Compliance, Quality Assurance, and Quality Control personnel • Quality,...
CfPA

Current Concepts in Cardiopulmonary Care - Atlantic City

This two-day course is geared to providing the new and experienced nurse, CRNA and respiratory therapist with a review of cardiopulmonary system pathophysiology along with common issues seen often in today’s environment. Also a review of heart failure, along with pulmonary hypertension, will be presented with common treatment plans. Finally, a discussion and presentation of sepsis and its effects on the heart and lungs will also be presented. PROGRAM LEARNING OUTCOMES This program prepa...
MED-ED

Applying Quality Risk Management

Who Should Attend? This online training will benefit professionals in the following industries: Medical Device, Pharmaceutical, Human Tissue, Biotechnology In departments such as: QA/QC/RA, Manufacturing/Operations, Research and Development, Legal. With job functions: Department managers and supervisors, QA/QC/RA specialists and engineers, Manufacturing and R&D engineers, chemists, scientists, formulators, documentation specialists, auditors, technicians. Course Description This 90-...
CfPA

Packaging Process Validations: Pharmaceutical and Medical Devices

Who Should Attend? This training is especially designed for personal involved with packaging process validations for pharmaceutical and medical devices packaging. Professionals in the following departments will benefit greatly from this training: • Package Engineering • Product Development • Manufacturing • Supply Chain/Logistics • Quality/Quality Assurance Course Description This intensive, 2-day course provides an overview for packaging validation practices....
CfPA

Packaging Pharmaceuticals, Medical Devices, and Combination Products

Who Should Attend? This training is designed for personnel involved with packaging for pharmaceutical, medical devices/combination devices, cosmetics, and personal care products. Departments may include: • Quality/Quality Assurance • Package Engineering • Supplier Development • Product Development • Logistics • Manufacturing Active participation and questions are encouraged throughout the course presentation. Course Description This 2-day intensive, accr...
CfPA

Aerosol Technology

Who Should Attend? This course will be of interest to those professionals who wish to develop an understanding of the most current developments in aerosol technology, as well as those who are actively involved in aerosol technology. This includes, but is not limited to: • Chemists • Engineers • Scientists • Technologists Course Description This course has been designed to cover the major aspects of aerosol technology and instruct you in the successful formulation of ...
CfPA

Controlled Crystallization of Organic Compounds

Who Should Attend? This course is intended for process chemists, chemical engineers, material scientists, project managers, consultants and other technical staffs responsible to ensure successful process development and/or production of organic compounds in pharmaceutical, food, fine chemical and cosmetics industries. Both experienced personnel and new-in-the-field can learn valuable concepts and be benefited from the course. Course Description Crystallization of organic compounds (such a...
CfPA

Surfactants: Chemistry, Theory, and Application

Who Should Attend? This course is designed for research and development and business area personnel engaged in a wide array of industries including architectural paints, industrial coatings, printing inks, adhesives, pharmaceuticals, agrochemicals, personal care products and cosmetics. It is targeted for formulation chemists as well as marketing, sales, and customer service personnel. Course Description This accredited, one day course on surfactants (chemistry, theory, and application) in...
CfPA

Rheology: Chemistry, Theory, and Application

Who Should Attend? This course is designed for research and development as well as business area personnel engaged in a wide array of industries including architectural paints, industrial coatings, printing inks, adhesives, pharmaceuticals, agrochemicals, personal care products and cosmetics. It is targeted for formulation chemists as well as marketing, sales, and customer service personnel. Course Description This course on rheology (chemistry, theory, and application) reviews the basic ...
CfPA

Drug Safety and Pharmacovigilance: A Comprehensive Course

Who Should Attend? This course is designed for professionals in the Pharmaceutical, Biotechnology, and related industries who work in the range of first in human clinical trials through and including post-marketing. It will be especially beneficial to individuals in the following areas: • Drug Safety/Pharmacovigilance (entry level to manager) • Clinical Operations (entry level to manager) • Quality Assurance (entry level to manager) • Regulatory Affairs (entry level to m...
CfPA

Non-Clinical Drug Safety Evaluation and Drug Development

Who Should Attend? This course is designed for a broad range of pre-clinical, clinical, management, investment, and regulatory personnel in both established and emerging pharmaceutical and biological companies. It will be of special value to: • Scientists who wish to gain an understanding of pharmaceutical toxicity studies • Safety Professionals • Regulatory Personnel • Managerial personnel • Early Clinical Project management staff • Regulatory Scientis...
CfPA

Developing Specifications for Drug Substances and Drug Products

Who Should Attend? This course is intended for those who want to improve their understanding of the overall process of developing specifications for drug substance and drug products from generic, OTC and research-based pharmaceutical industries. The course includes both basic and advanced level topics of interest to: • Pharmacists • Analytical and Pharmaceutical Chemists • Staff from Chemical Production Departments • QA and QC Professionals • Regulatory Affairs Per...
CfPA

How to Conduct Robust Root Cause Investigations for CAPA

Who Should Attend? This is an informative and interactive seminar for professionals in the pharmaceutical, biological, and medical device industries who conduct deviations, Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA) investigations, especially for professionals in the following disciplines: • Quality Control Analysts • R&D • Quality Assurance • Manufacturing • Product/Process Development • Engineering Course Description One of t...
CfPA

Drug Safety and Pharmacovigilance: A Comprehensive Course

Who Should Attend? This course is designed for professionals in the Pharmaceutical, Biotechnology, and related industries who work in the range of first in human clinical trials through and including post-marketing. It will be especially beneficial to individuals in the following areas: • Drug Safety/Pharmacovigilance (entry level to manager) • Clinical Operations (entry level to manager) • Quality Assurance (entry level to manager) • Regulatory Affairs (entry level to m...
CfPA

Non-Clinical Drug Safety Evaluation and Drug Development

Who Should Attend? This course is designed for a broad range of pre-clinical, clinical, management, investment, and regulatory personnel in both established and emerging pharmaceutical and biological companies. It will be of special value to: • Scientists who wish to gain an understanding of pharmaceutical toxicity studies • Safety Professionals • Regulatory Personnel • Managerial personnel • Early Clinical Project management staff • Regulatory Scientis...
CfPA

Qualification and Management of CMO’s

Outsourcing operations to CMO’s has become a critical segment of nearly every pharmaceutical company’s operational strategy, yet few clients or contractors achieve the envisioned expectations of these important relationships. The course examines the root causes of these issues which are much broader and deeper than technical capabilities. This practical course outlines both the strategic and tactical risk-based approaches for selecting, qualifying, monitoring, and managing CMO’s and o...
CfPA

Process Enhancement through Quality-by-Design

Who Should Attend? This course is especially designed for professionals in the pharmaceutical and biopharma industries. However, the course can easily be applicable to encompass food and chemical processing. Managers, Engineers, Analytical Scientists, Formulators, Purchasing Agents working in these industries will benefit greatly. It is applicable to departments such as Production, Analytical R&D, Quality Assurance, Quality Control, Pharmacy R&D and Purchasing/Budget Office. Course Descrip...
CfPA

Inpatient Obstetric Nursing Exam Review - Globe

Presented in lecture format, this course reviews topics for the National Certification Corporation (NCC) Examination “Inpatient Obstetrics.” Elements of the examination will be discussed, followed by a review of the content. Pictures, animation, and graphics will be utilized to enhance the presentation. The major components include disease processes during pregnancy, fetal evaluation, application of fetal monitoring for the laboring client, and postpartum and neonatal assessments. Practice...
MED-ED

Regulatory Compliance Basics for Medical Device, Pharmaceutical, Biologic, and Combination Product

Who Should Attend? Professionals in the Pharmaceutical, Biologic, Medical Device and Combination Products industries who will benefit most by attending this course include: • Senior management, RA, RC, QA, QC • Quality, Manufacturing, and Design engineers • Sales and Marketing, Maintenance, and Operational personnel, and Healthcare professionals, and • Anyone else who manages, assesses, or performs any related quality work. Course Description This 2-day accredite...
CfPA

Critical Care Concepts: Beyond the Basics - Anaheim

Although there are many programs available for those working in critical care, there is a need for those who are considered the “experts” to be challenged and further build their critical-thinking skills. With the constant changes in evidence-based practice driving what and why we do what we do, for many of us the only way to stay on top of the changes is through interaction in seminar format. Come learn, grow and be challenged as we move beyond the basics with the sickest of our patients....
MED-ED

Polymers in the Personal Care Industry

Who Should Attend? The short course will provide basic understanding of polymer chemistry, the similarities and differences, their functionality and how to best utilize this science to produce a better product. It will be especially valuable to personnel in the Cosmetic and Personal Care Industry within the following areas: • Formulation Development • Technical Service • Sales • Marketing Course Description This intense 90-minute accredited online training course wil...
CfPA

Digital Marketing Courses Pune | Training Institute | Affordable Fees

2 month advance digital marketing program by victorious digital at an affordable price with 100% placement assistance.
Digital marketing

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