Crestech Training Programs

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Classes begin in the 1st and 15th of the month.

Now offering the latest Oracle 9i hands on training to enable you to excel in the marketplace.


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.


Web Courses
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Web Design Diploma 400

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Web Graphics Design Certificate 240

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Web Development and Business Diploma 240

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Web Development and Business Diploma 450

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Web Development and Business Programming and Database Diploma

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JAVA Programming Specialist

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JAVA Programming Expert

Medical Courses
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Medical Assistant

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Medical Assistant Advanced

Crestech Top Courses
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PMI Project Management

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Business Analyst

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Web Graphics Design Diploma

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Oracle 9i Database Administrator

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InterNetworking Diploma

Database Courses
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Oracle 9i Database Administrator

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Oracle Application Developer

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Oracle Designer

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Datawarehousing Diploma

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E-Commerce Special

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!

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.

All training classes are offered in two formats: β€œhands-on” and β€œtraditional”. 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.

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.         

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
SAS $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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