Bites of Bitter PAI - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Bites of Bitter PAI


Pharmaceutical Technology
Volume 29, Issue 11

Two PAIs in the face


Control
"It was just after FDA had initiated the Pre-Approval Inspection process," reports our GMP Agent-in-Place. "We had put together a full PAI preparation process, including a policy and SOPs, all in a honking big binder along with pertinent checklists and FDA guidance, and all of which we sent to all of our US manufacturing sites. But management said that since our first PAI would be for 'just a topical product,' we didn't need to go through the full drill.

"Well, the inspectors came, they saw, and they didn't concur. The product failed and the inspectors slapped a withhold approval on us."

"We worked like dogs to make the necessary changes. We were making progress, but the Quality Department didn't think the site was quite ready yet. Then management stepped in again: they wanted us to amend NDA and request re-inspection now, 'Why not try it,' they said. 'If it works, we're ahead of the game. If not, we can fix it and go on.'

"So we got a second PAI," groused our Agent. "QA was right: we got another withhold approval, but this inspection cited procedures used at another site as well. So not only did we delay the launch of the topical product, but FDA also fired up a 'for cause' inspection of both sites. That inspection produced a warning letter. The warning letter cited us for discarding some original, raw data after the 'one year beyond dating period' required by the GMPs. NDA rules, however, say we have to retain the raw data at least until NDA approval...which we didn't have because we failed the first PAI.

"We did get approval in the end...years later. We needed to repeat studies we'd already done, because we'd destroyed the data.

"So much for 'just a topical product.'"

PAI in the dustbin

"The product was not a high priority, and the NDA had been filed seven years before FDA started the PAI process," recalls the responsible GMP Agent-in-Place. "And for the intervening seven years, we'd gotten no NDA questions. It was like we and FDA had both forgotten about it.

"And then FDA finally came.

"It was our first PAI ever at this site. The inspection was going well, but FDA required original development data to back up the reports, graphs, and tables submitted in the NDA. Now, this product had been developed under contract by a small lab a thousand miles away. When we tried to track them down, we found that the lab had closed and the researcher had died! Now, it may seem heartless, but we were desperate: we tracked down the widow...and she told us that she had trashed all of his work papers. She hadn't seen any need to keep them around, and, after all, when the research was done, there was no FDA requirement to archive this old data.

"Luckily, though, it was one of the first PAIs for our FDA inspector, too. And since the filing was very old, and since I talked myself hoarse trying to persuade him—without any company recognition, I might add—he finally accepted this explanation and gave us a pass.

"By the way, after all the delay and all the effort, we made 40 batches of the product to roll it out to the market, and sold only one of them in the two years before folding it."


ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
What role should the US government play in the current Ebola outbreak?
Finance development of drugs to treat/prevent disease.
Oversee medical treatment of patients in the US.
Provide treatment for patients globally.
All of the above.
No government involvement in patient treatment or drug development.
Finance development of drugs to treat/prevent disease.
28%
Oversee medical treatment of patients in the US.
9%
Provide treatment for patients globally.
9%
All of the above.
41%
No government involvement in patient treatment or drug development.
13%
Jim Miller Outsourcing Outlook Jim MillerCMO Industry Thins Out
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerFluorination Remains Key Challenge in API Synthesis
Marilyn E. Morris Guest EditorialMarilyn E. MorrisBolstering Graduate Education and Research Programs
Jill Wechsler Regulatory Watch Jill Wechsler Biopharma Manufacturers Respond to Ebola Crisis
Sean Milmo European Regulatory WatchSean MilmoHarmonizing Marketing Approval of Generic Drugs in Europe
FDA Reorganization to Promote Drug Quality
FDA Readies Quality Metrics Measures
New FDA Team to Spur Modern Drug Manufacturing
From Generics to Supergenerics
CMOs and the Track-and-Trace Race: Are You Engaged Yet?
Source: Pharmaceutical Technology,
Click here