Crestech Training Programs

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Course Materials
Crestech's Course Materials are designed to cover a broad and comprehensive range of clinical trials regulations, principles and practices, from basic principles to advanced and niche concepts including Pharmaceutical and Medical Device Ethical Standards, Human Research Subject's regulations, ICH and GCP guidelines, HIPAA, Regulatory and Source Documentation, Clinical Site Coordination & Monitoring.

 

Training Materials

Crestech distributes Inscape Publishing training products and materials. To view a list of training materials click a category below.

 

Attitudes Attitudes Listening Listening
Changes Change Managing Managing
Coaching Coaching Mentoring Mentoring
Communication Communication Personal Development Personal Development
Conflict Management Conflict Management Productivity Productivity
Creativity Creativity Sales Sales
Customer Relations Customer Relations Stress Stress
Diversity Diversity Supervisory Supervisory
Emotional Intelligence Emotional Intelligence Teamwork Teamwork
Innovation Innovation Teens Teens
Leadership Leadership Time Management Time Management

Course Materials
Crestech's Course Materials are designed to cover a broad and comprehensive range of clinical trials regulations, principles and practices, from basic principles to advanced and niche concepts including Pharmaceutical and Medical Device Ethical Standards, Human Research Subject's regulations, ICH and GCP guidelines, HIPAA, Regulatory and Source Documentation, Clinical Site Coordination & Monitoring, 

 



Adverse Events Reporting and Recent Case Histories. This course uses a diverse set of online and textbook-based training modules. Students are encouraged to complete all of the available Certificate programs, but are free to complete as many or as few of the modules as they desire. 
 



Two optional sets of material (CCRP's Certificate Program and Duke University's training manual, described below) are available at an additional cost. All other materials are included in the standard course. Please discuss with us which options best suit your needs.



Crestech is collaborating with Thomson CenterWatch as a provider of the two core textbooks for this course. Their CRC and CRA Guides cover the 2 most common job functions that our class participants target, and are ideal companions for Crestech's proprietary skills-based instructor-led training. You can read more about CenterWatch following the two textbook descriptions below.


 

 

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Full list of courses and prices

Crestech is proud to be a neighbor of Novartis corporation, literally a stone throw away from the  building of Novartis in East Hanover, New Jersey. Novartis employees are clients of ours, and are very proud of being a part of  Novartis Preferred Vendor program.
 


Crestech Training is a premier provider of technical support and training to the pharmaceutical and allied health sciences industries. Since 1994 we have been helping pharmaceutical and healthcare companies solve problems related to analytical method development and optimization, analytical testing, and laboratory staff training.

With a strong technical background in chemical analysis, process optimization, systems development, and teaching, we can address both simple and complex technical issues. Our global approach centers on understanding the entire problem, and then designing a solution that meets your unique needs. We are successful because we ask questions, listen to your answers, and then work with you to develop the best solution.

Our clients have a wide variety of needs. Sometimes that need involves providing additional technical support for a critical project, or a review of important documents prior to a regulatory submission. Often we are part of a team trying to solve a multi-disciplinary problem. Other clients may need the long-term technical commitment that only Crestech can provide, while some may need a cost-effective way to train their technical staff, without sending them off-site.

Crestech can access an extensive network of technical resources. We can provide the expertise that you need, when and where you need it. Our many affiliated laboratories can also provide analytical testing when necessary. Integrated resources provide an integrated solution!
 

FAQs about Customized Training

What is "Customized Training"?

"Customized Training" is the process of tailoring training to your organization's needs either by adapting an existing program or developing a new program. The customization process allows us to focus the content and the learning activities to get the most impact for your training dollars. We can customize one of our existing programs or develop a course for you from the ground up.

Does Crestech know my business well enough to customize training for me?

You know your business better than we do. Crestech works with you and other experts in your company to define the profile of your learners and how the training content will improve their performance and help the organization meet its goals.

Can Crestech convert an existing program to another delivery method?

New advances in training technology continue to expand the choices available for training. Programs that were traditionally instructor-led can now be blended with interactive multimedia, web-based discussions or totally converted to computer-based training. Crestech can help you determine the most effective way to deliver your material.

What components of an existing program can you customize?

The most commonly customized components are the learning activities, which can range from case studies to role-plays to specially designed problems. The length of the program, the types of learners and your learning objectives help define what areas are customized. Of course, we can expand or revise content to address specific organizational objectives, as well.

What types of programs can be customized?

Crestech specializes in healthcare organizations. Our network includes business, clinical and instructional experts who can help you meet your organizational goals. If we don't have the right team to customize for your project, we will help you find someone who does.  Customization includes delivery method, content, location and the length of the class.
 

The Center for Professional Advancement: Professional Training for Pharmaceutical Training, Biopharmaceutical Training, Chemical Engineering Training, Continuing Professional Education, Technical Training, GMP Training, FDA Regulations, Clinical Research Training, Onsite Training

 

We provide Pharmaceutical Training

Crestech is in the heart of the Pharmaceutical Industry in the center of the Garden State. Knowledge transfer to the workforce is key to success. Our Oracle, Clintrial and other courses are designed to quickly deliver the critical level of training needed by Clinical Research Coordinators (CRCs) & Monitors (CRAs). 


  
Crestech's specialized programs are appropriate for managers, students, new clinical staff, recent college grads, or career-changing professionals looking to advance in the Clinical Trials industry. The courses concentrate on the "Four P's": policies, procedures, principles, and practices of Clinical Studies and consists of 40 hours (5 days) of instructor-led training followed by 40 hours of self-study.
 


This course gives a brief overview of all the modules in Clintrial, but the main focus is on the Enter and Retrieve modules.  This course is recommended for data entry personnel who will be entering and retrieving the patient data.  The course includes various aspects of data entry, including the types of data entry, navigation, setting up user preferences and creating flags and note.
         

All training classes are offered in two formats: The hands-on training classes are often ideal for small groups; using standard or site-specific specifications, SOPs and CRFs, ClinicalSoft instructors will demonstrate how to design and utilize clinical and safety systems effectively and efficiently. The traditional classes are presented in a lecture format and include a number of hands-on exercises to apply theoretical product knowledge.


 

New Course List Cost Hours
PHARMACEUTICALS FDA-cGMP TRAINING $4000 8/16/80
ISO 9000:2000 TRAINING $4000 8/16/80
ISO 14000:1996 and Environmental Standard Training $4000 8/16/80
ISO 14000:1996/ISO 19011 AUDITOR TRAINING $4000 8/16/80
ISO/TS 16949:2002 TRAINING $4000 8/16/80
FDA-cGMP TRAINING (Quality System Requirements -21CFR820) $4000 8/16/80
ISO 9000:2000/ISO 19011 AUDITOR TRAINING $4000 8/16/80
ISO 13485:2003 TRAINING $4000 8/16/80
Adverse Events: Reporting and Managing $4000 8/16/80
Anatomy & Physiology $4000 8/16/80
Basic ECG Interpretation $4000 8/16/80
Bioterrorism: A Public Health Challenge $4000 8/16/80
Caring For Your Patients As If Their Real Lives Mattered $4000 8/16/80
Cognitive Therapy: Interventions for Healthcare Providers $4000 8/16/80
Customer Service for Nursing $4000 8/16/80
Cultural Competence in Healthcare $4000 8/16/80
Cyclothymia: Through the Patients Eyes $4000 8/16/80
Documentation: Best Defense is Good Offense $4000 8/16/80
Humor and Health $4000 8/16/80
Infection Control: Controlling Those Invisible Microbes $4000 8/16/80
Infusion Therapy Certification and Training $4000 8/16/80
Introduction to Pharmacology: Concepts & Terminology $4000 8/16/80
Laboratory Findings: More Than Just Numbers $4000 8/16/80
Latex Allergy: Are You Risking Your Life? $4000 8/16/80
Mastering Managed Care and Health Insurance $4000 8/16/80
Medical Terminology (Online) $4000 8/16/80
Medical Terminology (Basic) $4000 8/16/80
Medical Terminology (Introduction) $4000 8/16/80
Medical Terminology (Advanced) $4000 8/16/80
Pain Management $4000 8/16/80
PICC/Midline Certification and Training $4000 8/16/80
Preventing Medication Errors $4000 8/16/80
Risks of Anesthesia $4000 8/16/80
Taking the Sting Out of Shots: Pediatric Immunizations $4000 8/16/80
The Perinatal Nurses Role in Supporting Breast Feeding $4000 8/16/80
The Rapidly Changing World of Your Elderly Patients $4000 8/16/80
Adventures in Attitudes $4000 8/16/80
Behavioral Interviewing $4000 8/16/80
Coaching $4000 8/16/80
Coaching Job Skills $4000 8/16/80
Communicating Up $4000 8/16/80
Customer Service for Nursing $4000 8/16/80
Dealing with Complaints $4000 8/16/80
Dealing with Conflicts $4000 8/16/80
Delegating $4000 8/16/80
Developing Performance Goals and Standards $4000 8/16/80
DiSC Dimensions of Leadership $4000 8/16/80
DiSC® Management Strategies $4000 8/16/80
Effective Discipline $4000 8/16/80
Effective Team Management $4000 8/16/80
Essential Skills of Communicating $4000 8/16/80
Essential Skills of Leadership $4000 8/16/80
Improving Work Habits $4000 8/16/80
Innovate with C.A.R.E. now Team Dimensions® $4000 8/16/80
Leadership Professional Certificate Program $4000 8/16/80
Managing Difficult Personalities $4000 8/16/80
Managing Performance Discussions $4000 8/16/80
Performance Assessment $4000 8/16/80
Reinforcing Your Understanding of Behavioral Styles $4000 8/16/80
Reinforcing Your Understanding of Behavioral Styles for Managers $4000 8/16/80
Reinforcing Your Understanding of Behavioral Styles Teams $4000 8/16/80
Supervision Series $4000 8/16/80
Supporting Change $4000 8/16/80
Team Dimensions $4000 8/16/80
Transition: The Personal Path Through Change $4000 8/16/80
Understanding Behavioral Styles $4000 8/16/80
Understanding Behavioral Styles for Managers $4000 8/16/80
Understanding Behavioral Styles for Teams $4000 8/16/80
Work Expectations Profile® $4000 8/16/80
Adult Ventilation Management $4000 8/16/80
Project Management for Pharmaceutical Industry  $4000 8/16/80
Continuous Improvement for Pharmaceutical Industry $4000 8/16/80
Oracle Clinical $4000 8/16/80
Quality Assurance for the Pharmaceutical Industry $4000 8/16/80
Design of Experiments for the Pharmaceutical Industry $4000 8/16/80
Custom Reports $4000 8/16/80
Biopharmaceutical Training $4000 8/16/80
Chemical Engineering Training $4000 8/16/80
GMP Training $4000 8/16/80
Clinical Research Training, and other Technical and Onsite Training. $4000 8/16/80
Reg GMP for Management $4000 8/16/80
Clinical Trial GCP Basic $4000 8/16/80
Clinical Trials GCP Intermediate $4000 8/16/80
Clinical Trials GCP Advanced $4000 8/16/80
Medical Devices GMP Basic $4000 8/16/80
Medical Devices GMP Intermediate $4000 8/16/80
Medical Devices GMP Advanced $4000 8/16/80
API Equipment Understanding $4000 8/16/80
API Process Understanding $4000 8/16/80
Finished Dose Validation $4000 8/16/80
Finished Dose Equipment $4000 8/16/80
Aseptic Process Introduction $4000 8/16/80
Microbiology Lab GMP $4000 8/16/80
Microbiology Lab Practices $4000 8/16/80
Analytical Lab Application $4000 8/16/80
Analytical Lab Practices $4000 8/16/80
Analytical Lab GMP $4000 8/16/80
GVC: Computer use and application $4000 8/16/80
PVC: Health and Safety General $4000 8/16/80
Pharma GMP Basic $4000 8/16/80
Pharma GMP Intermediate $4000 8/16/80
Computer & Software Validation $4000 8/16/80
Laboratory Equipment Qualification $4000 8/16/80
Qualified Person in Clinical Trials $4000 8/16/80
Stability Testing for pharmaceutical products $4000 8/16/80
Managing and Reporting Process Deviations and GMP Failure Investigations $4000 8/16/80
Fast Track Guide to the Pharmaceutical Industry $4000 8/16/80
Clinical Trial Directive $4000 8/16/80
Developing Global Pharmaceutical Pricing Strategies $4000 8/16/80
Carrying out Batch Record Review and Product Release $4000 8/16/80
Technology Transfer $4000 8/16/80
Stability Testing for Biotechnology Products $4000 8/16/80
Ensuring compliance with the regulations surrounding sampling of Raw Materials $4000 8/16/80
Ensuring compliance with the regulations surrounding sampling of Raw Materials $4000 8/16/80
Water Validation $4000 8/16/80
FDA Requirements for Packaging and Labelling $4000 8/16/80
Regulatory Affairs for Generics $4000 8/16/80
Medical Writing $4000 8/16/80
Regulatory Affairs Strategies
 
$4000 8/16/80
Preparing the Chemistry and Pharmacy Section of the EU Registration Dossier $4000 8/16/80
Introduction to pharmacokinetics for the non-specialist $4000 8/16/80
Qualified Person in Clinical Trials $4000 8/16/80
Introduction to European Regulatory Affairs $4000 8/16/80
Advanced-level Adverse Event Reporting & Pharmacovigilance $4000 8/16/80
Signal Detection Strategies $4000 8/16/80
Understanding US-FDA Drug Submission Procedures $4000 8/16/80
Mastering EU Requirements for Product Labelling & Package Leaflets $4000 8/16/80
Fast Track Guide to the Pharmaceutical Industry $4000 8/16/80
Filing Variations $4000 8/16/80
Regulatory Affairs for Biotechnology
$4000 8/16/80
Adverse Event Reporting and Pharmacovigilance $4000 8/16/80
Regulatory Affairs for Central & Eastern Europe $4000 8/16/80
Stability Testing for Biotechnology Products $4000 8/16/80
Introduction to Regulatory Affairs for Biotech $4000 8/16/80
Medical Writing $4000 8/16/80
Introduction to Toxicology for the Non-specialist $4000 8/16/80
Writing and Managing SOPs for Clinical Quality Assurance $4000 8/16/80
Introduction to pharmacokinetics for the non-specialist $4000 8/16/80
Qualified Person in Clinical Trials $4000 8/16/80
Clinical Research Project Management $4000 8/16/80
Clinical Statistics for the Non-Statistician $4000 8/16/80
Fast Track Guide to the Pharmaceutical Industry $4000 8/16/80
Monitoring Clinical Trials for GCP Compliance $4000 8/16/80
Developing a Balanced Scorecard for Clinical Operations $4000 8/16/80
Clinical Trial Directive $4000 8/16/80
Medical Writing $4000 8/16/80
Introduction to Toxicology for the Non-specialist
 
$4000 8/16/80
Introduction to Toxicology for the Non-specialist
 
$4000 8/16/80
Clinical Research Project Management $4000 8/16/80
Fast Track Guide to the Pharmaceutical Industry $4000 8/16/80
Clinical Trial Directive $4000 8/16/80
Pharmaceutical Licensing $4000 8/16/80
Mastering Real Options Evaluation & Risk Analysis $4000 8/16/80
Regulatory Affairs for Biotechnology $4000 8/16/80
Stability Testing for Biotechnology Products $4000 8/16/80
Introduction to Regulatory Affairs for Biotech $4000 8/16/80
Pharma GMP Advanced $4000 8/16/80

 

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