Managing Recipe Process Definitions and Manual Processes

by | Jul 14, 2008 | Uncategorized

Jim Cahill

Chief Blogger, Social Marketing Leader

One of my Google blog search RSS feeds on batch processes alerted me to an article, The New Recipe for Pharma Success. It describes how many Life Sciences manufacturers use low-tech tools like spreadsheets, flow charts, and other unstructured documents to create and maintain the process definitions. It concludes:

Bottom line, unstructured documents needlessly increase expenses and prolong time to market. Bad data may be introduced–or good data may be overlooked–at any stage of the product lifecycle, requiring companies to repeat one or more stages.

I ran this post by Joanne Salazar (perspective21 for you Twitterers out there.) Joanne has many years of experience with Emerson and is extremely knowledgeable of the regulatory compliance challenges pharmaceutical and biotech manufacturers face. She is currently focusing her efforts on the Compliance Suite manufacturing operations software, which joined the Emerson family last summer.

Joanne wrote back such a great reply, I thought it best to include in its entirety:

Pharma companies spend lots of money and lose valuable time bringing drugs to market as the patent expiration dates move ever closer. The data involved in defining the “recipe” for the drug is voluminous and needs to be managed throughout its lifecycle. Companies are gaining efficiencies to quickly startup production facilities in several ways:

  • integrating change control between development and operations as a drug facility is brought online
  • creating reusable libraries of process operations using S88 and S95 standards as a basis
  • integrating commissioning and qualification efforts
  • using .NET framework to minimize validation efforts, by ensuring functionality of applications once then deploying to various clients

In regards to managing the information and documentation, several additional practices are evolving:

  • more structured documents upstream in the drug development cycle enable pertinent data to be easily imported into manufacturing systems – resulting in faster time to market
  • the technology and ability to easily interface various systems in a manner that is maintainable is becoming a reality due to S95 and other standards; therefore, pharma manufacturers can readily produce a complete electronic batch records that include recipe, formulas, manual, and automated actions, comments, required data to be gathered during processing, prompts, alarms, deviations, signatures, approvals, etc.
  • easily accessing current and approved reference documents (SOP, MSDS) for plant floor work instructions to ensure proper actions are taken
  • verifying the training certification of operators at point of action
  • managing documents throughout their life cycle: document check-in and check-out, version management, automatic routing, storage, single- and multi-document change control, archived records management, and printing

Helping process manufacturers solve these documentation, maintainability, training and change management challenges is simplified with software like Compliance Suite and project teams who can automate these manual processes.

Popular Posts


Subscribe for Updates

Follow Us

We invite you to follow us on Facebook, LinkedIn, Twitter and YouTube to keep up to date on all the latest news, events and innovations to help you take on and solve your toughest challenges.

Want to re-purpose, reuse or translate content?

Please do, Just link back to the post and send us a quick note so we can share your work. Thanks!

Our Global Community

Emerson Exchange 365

The opinions expressed here are the personal opinions of the authors. Content published here is not read or approved by Emerson before it is posted and does not necessarily represent the views and opinions of Emerson.