Seminar on Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)

Course "Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:

Writing SOPs or procedural documents can be challenging at times. However, writing SOPs is overall a straightforward process. However, enforcing what you already created and implemented in the pipeline is another story. The term SOP is very obvious. We have seen "clearly written description of how specific tasks are to be done." 

Who Will Benefit:

This Seminar will provide valuable assistance and guidance to pharmaceutical, medical device and biotechnology manufacturers and other firms in the life sciences industry who require a refresher session on writing and enforcing their own SOPs and internal procedures or for those new to this area who desire to gain a better understanding of the SOP process. The employees who will benefit include basically anyone and everyone at your organization who are required to write and/or comply with SOPs, including all levels of management and departmental representatives and those who desire a better understanding or a "refresh" overview of the SOP process from start to finish, including:

• Regulatory Affairs
• Clinical Affairs
• Quality Assurance/Quality Control
• Compliance
• Marketing & Sales
• Manufacturing and Technical Services
• Engineering
• IT/MIS
• Executive Management
• Laboratory Operations
• Customer Service
• Clinical Research managers and personnel
• Specialists/SMEs in all departments
• QA/RA managers and personnel
• Quality System auditors
• Distributors/Authorized Representatives
• Legal Counsel
• Consultants

Speaker:

David R. Dills

Regulatory Affairs & Compliance Consultant, 

David R. Dills, Regulatory & Compliance Consultant with more than 24 years of hands-on experience and a proven track record within the FDA regulated industry, has an extensive regulatory and compliance background with Class I/II/III and IVD devices, pharmaceutical operations, and manages activities within the global regulatory and compliance space. 

Location: Philadelphia, PA Date: May 12th & 13th, 2016 Time: 9:00 AM to 6:00 PM

Venue: Hilton Garden Inn Philadelphia Center City

Address: 1100 Arch Street, Philadelphia, Pennsylvania, 19107, USA

Price:

(Without Stay) Price: $1,295.00 (Seminar for One Delegate)

Until March 31, Early Bird Price: $1,295.00 from April 01 to May 10, Regular Price: $1,495.00

(With Stay) Includes Price: $1,695.00 (Seminar for One Delegate)

Until March 31, Early Bird Price: $1,695.00 from April 01 to May 10, Regular Price: $1,895.00

Quick Contact:

NetZealous DBA as GlobalCompliancePanel

Phone: 1-800-447-9407

Fax: 302-288-6884

Email: support@globalcompliancepanel.com      

Website: http://www.globalcompliancepanel.com/

Registration Link - http://bit.ly/writing-enforcing-effective-SOPs-Philadelphia