Cart

Contains 0 items
Total: $0.00
View Shopping Cart

Toll Free:
+1-888-717-2436

Hitech, Aerospace and Manufacturing Regulations Training, Compliance Best Practices and Standards

Hitech, Aerospace and Manufacturing regulations based webinars, in-person seminars, standards and best practices. Learn from renowned experts about regulations affecting the high-technology, aerospace and manufacturing industries - ISO 9001:2000, AS9100, ISO 9001:2008, ISO 19011, FAA Safety Management System, FAA SMS Regulations Training, Accelerated Life Tests, Statistical Process Control, Advanced Product Quality Planning (APQP), etc.

Sub Categories: Quality & Safety | Standards and Methodology

Best Sellers

Webinars
Seminars
Standards

Pharmaceutical Compressed Air - Quality GMP Standards and Requirements
By: Roger Cowan
Price: $249
Add to Cart
How to Conduct a HIPAA Risk Assessment
By: Brian Tuttle
Price: $249
Add to Cart
Building a Vendor Qualification Program for FDA Regulated Industries
By: Jonathan M Lewis
Price: $249
Add to Cart
FDA Regulations for Marketing OTC Drugs in the U.S.
By: Norma Skolnik
Price: $249
Add to Cart
Effective Annual U.S. FDA CGMP Training
By: John E Lincoln
Price: $249
Add to Cart
CDISC Mapping 1: Specifications and FDA Requirements
By: Sunil Gupta
Price: $249
Add to Cart
Extractables and Leachables in Early Phase Development
By: Wayland Rushing
Price: $279
Add to Cart
Veterinary Medicine and the DEA Due Diligence Requirement for Dispensing and Prescribing...
By: Carlos Aquinos
Price: $229
Add to Cart
1099 & W-9 Update - Complying with IRS Information Reporting Guidelines
By: Miles Hutchinson
Price: $149
Add to Cart
OSHA Recordkeeping for 2015: Beyond the OSHA 300 Summary
By: David A. Casavant
Price: $149
Add to Cart
Form I-9 and E-Verify, getting and staying compliant
By: Cathleen Hampton
Price: $149
Add to Cart
Affordable Care Act Updates: What Employers need to do to Prepare
By: Vanessa G Nelson
Price: $149
Add to Cart
Child Support: What Payroll Doesn't Know Can Hurt You
By: Vicki M. Lambert
Price: $229
Add to Cart
Detecting and Preventing Embezzlement in Your Organization
By: Peter Goldmann
Price: $249
Add to Cart
What Employers Need to Know About Severance Agreements
By: Janette Levey Frisch
Price: $229
Add to Cart

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance: 2-Day In-Person Seminar

San Francisco, CA | Dec 6-7, 2018
Add to Cart
FDA's New Import Program for 2017 - Strict Precision: 2-Day In-Person Seminar by Ex-FDA Official

Boston, MA | Nov 8-9, 2018
Add to Cart
Critical Vendor Risk Management: Exclusive One and a Half-day Boot Camp

Chicago, IL| Nov 8-9, 2018
Add to Cart
21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-day In-person Seminar

Philadelphia, PA | Oct 18-19, 2018
Add to Cart
Quality Control Laboratory Compliance - cGMPs and GLPs: One and a Half-day In-person Seminar

San Francisco, CA | Nov 15-16, 2018
Add to Cart
Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizati...

San Francisco, CA | Nov 15-16, 2018
Add to Cart
Latin America: Regulatory Compliance Requirements for Life Science Products...

San Diego, CA | Nov 28-29, 2018
Add to Cart
Computer System Validation - Reduce Costs and Avoid 483s: 2-Day In-Person Seminar

Philadelphia, PA| Oct 18-19, 2018
Add to Cart
FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials: 2-Day In-Person Seminar by Ex-FDA Official

Tampa, FL| Dec 6-7, 2018
Add to Cart
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and...

Boston, MA| Nov 1-2, 2018
Add to Cart
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

Orlando, FL | Nov 8-9, 2018
Add to Cart
China & Pacific Rim Markets : Compliance Processes for Life Science Products...

San Francisco, CA | Jan 24-25, 2019
Add to Cart
Vendor and Supplier Qualification Program for FDA Regulated Industries: 2-Day In-Person Seminar

San Diego, CA| Dec 13-14, 2018
Add to Cart
Designing and Sustaining New and Existing Product Stability Testing Program

Orlando, FL | Oct 18-19, 2018
Add to Cart
HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Offi...

San Diego, CA | Nov 15-16, 2018
Add to Cart

General requirements for the competence of testing and calibration laboratories
Provider: ANSI
Price: $142
Add to Cart
IEC 62304:2015 ''Medical Device Software - Software Life Cycle Processes''
Provider: SEPT
Price: $299
Add to Cart
IEC 62304:2015 ''Medical Device Software - Software Life Cycle Processes''
Provider: SEPT
Price: $149
Add to Cart
ISO 13485 Procedure 754-Customer Property
Provider: 13485 Store
Price: $12
Add to Cart
Measurement management systems - Requirements for measurement processes and measuring equipment
Provider: ANSI
Price: $120
Add to Cart
Geometrical Product Specifications (GPS) - Geometrical tolerancing - Tolerances of form, orientation...
Provider: ANSI
Price: $250
Add to Cart
Templates and Plans for Software Configuration Management Documents-Version 6.0
Provider: SEPT
Price: $299
Add to Cart
Computer System Validation Master Plan
Provider: LabCompliance
Price: $90
Add to Cart
Zero Acceptance Number Sampling Plan for Receiving, In-Process and Final Inspection
Provider: Quality-Control-Plan
Price: $37
Add to Cart
Standard Operating Procedure: FDA Inspections
Provider: LabCompliance
Price: $49
Add to Cart
AS9003 Comprehensive Quality System Kit for Inspection and Test Quality Control System
Provider: At-PQC
Price: $397
Add to Cart
ISO 13485 and FDA Compliant Internal Audit Tools: Checklist, Procedure and Forms
Provider: 13485 Store
Price: $95
Add to Cart
Template for a Software Maintenance Plan - Fourth Edition
Provider: SEPT
Price: $99
Add to Cart
Sarbanes Oxley Treasury Risks and Controls
Provider: Audit Net
Price: $50
Add to Cart
ISO 13485 Gap Checklist
Provider: 13485 Store
Price: $59
Add to Cart

You Recently Viewed