Webinar Sneak Peek: Changing from Paper-Based to Electronic Manufacturing

Click here to register. Register before 10/1/2016 and use the code earlybird to attend for free! Related Posts:InstantGMP, Inc. Announces Webinar: Changing from…DemoGMP Compliance CostWebinar: Federal, State and Self-Regulation of E-cigarettesWhite PapersNew Approach for a New Start-Up: Innovative Formulations…

InstantGMP, Inc. Announces Webinar: Changing from Paper-Based to Electronic Manufacturing of FDA Regulated Products

Cary, NC – The Quality and Manufacturing experts from InstantGMP, Inc. will be conducting a webinar on October 4th, 2016 entitled “Changing from Paper-Based to Electronic Manufacturing of FDA Regulated Products”. Despite all the technology we use to automate our daily lives, manufacturing documentation remains paper-based and can cause many problems from cross-departmental miscommunication, redundancies,[…]

InstantGMP Vape, Vape Mentors and EAS Consulting to Host Webinar on E-cigarette Regulations

InstantGMP Vape is teaming up with Vape Mentors and EAS Consulting to host a webinar on Federal, State and Self-Regulation of the e-cigarette industry. With federal regulations on the horizon and states enacting their own legislation, the industry is in a state of constant change.  Committed e-liquid manufacturers have taken steps to self-regulate and lead[…]

Webinar Preview: Capturing Processes for MBRs

Webinar Preview: Capturing Processes for MBRs On Tuesday, April 21st, InstantGMP and dietary supplement regulatory expert Marian Boardley present Tips for GMP Compliant Master Batch Records. There’s still time to sign up! We will be sharing common issues with Master Batch Records that lead for 483s and how you can avoid them.   MBRs are[…]

InstantGMP and Marian Boardley Present Webinar: GMP Compliant Master Batch Records

Cary, NC – In 2014, nearly 10% of 483 observations by the FDA stemmed from issues with Master Batch Records. Improving Master Batch Records can reduce 483s, make completing your batch records easier and ultimately improve the quality of dietary supplements. InstantGMP teams up with consultant Marian Boardley to share advice on writing Master Batch[…]

SOPs: The Foundation of an FDA regulated Quality System

SOPs, or Standard Operating Procedures, are integral to a complete quality system for your dietary supplement manufacturing facility.  SOPs provide specific instructions for completing an operation and are based on Policies, which are controlled documents that guide the executive management team towards compliant business practices. Implementing SOPs throughout the manufacturing process will ensure that you[…]

Webinar Preview: The Foundation of a Quality System and Implementing SOPs

Next Tuesday, InstantGMP and EAS Consulting Group present SOPs: The Foundation of a Quality System. There’s still time to sign up! We will be sharing helpful information on SOPs including the outline of an SOP and examples of how SOPs are applied throughout the manufacturing process. Webinar Preview: Implementation While the overall purpose of implementing[…]

Manufacturing Facility Webinar on Standard Operating Procedures

Cary, NC – With the quality and purity of dietary supplements recently being called into question, establishing a quality system is paramount to ensuring products are safe. Writing Standard Operating Procedures (SOPs) is the first step in creating this system for a manufacturing facility. InstantGMP and EAS Consulting Group will host a webinar, “SOPs: The[…]

GMP Certification Webinar Preview: Finding a Reputable 3rd Party Certification Organization

Finding a Reputable 3rd Party Certification Organization InstantGMP’s Prepare for GMP Certification webinar is just days away! Gretchen Rizor, our Support Specialist and Quality expert,  will share helpful information on the process for GMP certification and how to prepare your supplement manufacturing facility for a GMP audit. The webinar will take place on Tuesday, January[…]