Qtech-Sol Professional Development Center LLC (QPDC) is a Professional Training Organization. QPDC is a Private Vocational School and its Clinical Science
Programs are approved by Department of Education and Department of Unemployment and Workforce Development, New Jersey, USA and we are listed on New Jersey
Eligible Training Provider List since year 2011.
We develop various Job Specific Training and Workshop programs primarily focusing towards Clinical Science, (Clinical Research, Drug Safety, Clinical Data Management),
Healthcare Business and SAS Reporting and Analytics Practices. We help professionals and students to opt for the best career pathway per their education. QPDC's Staff and
Professional advisors bring their scientific, regulatory and informative management experience to deliver timely, accurate, cost-effective programs ,which will help its users
to apply the learning direct into business. Our headquarters in New Jersey and regional office in India. Our Objective is to provide the best practices followed in industry
with various exercises to support student delivery. At the end of the workshop a certificate of completion is provided to each participant by QPDC.
All Workshop conducted is a 3 Day session with Online material access.
- Day-1 : Faculty based presentation and concept delivery
- Day-2 : Includes concepts on Exercise for delivery
- Day-3 : Includes review of the submissions and query addressing
Each of the Workshop is conducted via WebEx (online) and is supported with following Online material for student learning and delivery for each workshop conducted.
- Lesson Presentation
- Multiple Choice Objectives (MCQs)
- Discussion based Questions
- Exercises with Data Inputs
Clinical Research Associate Training and Workshop Learning's
The candidate will be working on various workshops to perform the following tasks. Case 1: Introduction To Clinical Trial , Case 2: FDA EMEA Regulations ,
Case 3: Institutional Review Board (IRB) ,Case 4: Protocol Design and Development, Case 5: Clinical Trial Budget , Case 6: Case Report Form (CRF) Design ,
Case 7: Investigator Meeting , Case 8: Site Management and Initiation , Case 9: Informed Consent Preparation , Case 10: Trial Master File ,
Case 11: Adverse Event Monitoring and Reporting, Case 12: Clinical Trial Audit
Drug Safety Associate Training and Workshop Learning's
The candidate will be working on various workshops to perform the following tasks. CASE 1. Introduction to Adverse Events , CASE 2. Role of DSA,
CASE 3. Characteristics of Case , CASE 4. Medical Record Extraction, CASE 5. Basics of Coding , CASE 6. Triage, CASE 7. Case Narratives , CASE 8. SAE Reconciliation,
CASE 9. Drug Safety Database and Software AND Other workshop learning on Medical Record Extraction , Adverse Events Case Processing, CIOMS Line Listing ,
Case processing and FDA Reporting for Medical Devices, Revision of SOP Quality Control Procedure, SAE Reconciliation, PSUR - Periodic Safety Update Reporting,
Triage, Data Entry, Signal Detection, Labeling Edit check, Quality Control Procedure, Resolution of queries of pending cases , SUSAR - Suspected Unexpected Serious
Clinical Data Management Training and Workshop Learning's
The candidate will be working on various workshops to perform the following tasks. CASE 1. Introduction to Clinical Trials, CASE 2. Protocol Design and
Development, CASE 3. Data Management Plan, CASE 4. Data Cleaning and Data Validation., CASE 5. Query Management, CASE 6. Coding of Adverse Events,
CASE 7. SAE Reconciliation., CASE 8. Elements of CRF, CASE 9. e-CRF designing, Data tracking from CRF.
Clinical SAS Oriented - Data Management Workshop Learning's
The candidate will be working on various workshops to perform the following tasks. (1) SAS Efficiency Programming (2) Data based Validation
(3) Protocol based Validation (4) Pharmacokinetics and Pharmacodynamics (5) Preparing Analysis Datasets CDISC (6) Oncology project Phase-I
(7) Ophthalmology Project Phase-II (8) Cardiology Project Phase-III (9) Central Nervous System (CNS) Project (Phase-IV)(10) Aggregate Reporting Process
(Pharmacovigilance) (11) Open CDISC Validation.
Healthcare Business Analyst Workshop Learning's
The candidate will be working on various workshops to perform the following tasks. (1) Overview of US Healthcare system (2) Healthcare Claims
(3) Healthcare Claims Forms (4) Public Health Coverage (5) HIPAA - Health Insurance portability and Accountability Act (6) International Classification of
Diseases (ICD) (7) Healthcare Codes (8) Overview of Medicaid Management Information System (MMIS) (9) NCPDP - National Council for Prescription Drug Product
(10) Healthcare Data warehouse.