GlobalCompliancePanel onsite training allows you the freedom
to choose the format and manner in which you want our Experts to offer their
experience. You can choose to have them come over to your place, or you could
delegate personnel from your organization to interact with them, or they can be
assigned to your organization for a set period of time till your issues are
resolved.
On-Site Training Benefits
Schedule at Your Convenience
Time Efficient
Cost Efficient
Customized Course Selection
Best Results
Team Building
Choose by
Areas:
- 21
CFR Part 11
- Analytical
Development and Formulation, Drug Process Development
- Audit
Preparation
- Bianalytical
method development
- Bioresearch
- Clinical
Research / Drug-Device Development
- Clinical
trial
- Contract
Manufacturing Compliance
- FDA
Audit & Inspection
- FDA
quality system
- Food
Safety
- GCP
compliance
- Global
Regulatory Submission
- Immunogenicity
and Bioassay Method Development
- IND,
IDE, CAPA, GMP/cGMP Compliance & PMA's
- ISO
13485/EN46000 and ISO 9000
|
- Laboratory
Testing
- Lean
Manufacturing
- Manufacturing,
Packaging and Labeling
- Microbial
control in Clean rooms and other critical environments
- Microbiology
and sterilization
- Operational
risk management, risk frameworks
- OSHA
and MSHA litigation
- Pre-marketing
tPost-marketing
- QMS
Process & Maintenance
- Quality
and process development
- Quality
Systems and Laboratory Controls
- Risk
Management
- Software
Validation/Verification
- Supply
chain development and management
- Toxicology
- Water
systems, sterilization, aseptic processing
|
Request for Quote
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Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.
Phone: +1-800-447-9407
Fax your PO to: 302 288 6884
http://www.globalcompliancepanel.com/
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