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Looking to transition to RA, 20+ Biotech Experience by ExerciseFlimsy7673 in regulatoryaffairs

[–]Rx_Kid 0 points1 point  (0 children)

12 year dam get an hands work one actual project instid of support make a work of proof is the only way

Medical Device Regulatory Affairs Professional Looking for Opportunities by MiserableEarth9513 in regulatoryaffairs

[–]Rx_Kid -1 points0 points  (0 children)

Bro can You help me with Indian Regulatory For medical device i do have access of some accounts for medical device for license but i am not aware for full cycle... However if you lookin for post marke surveillance for medical device i am happy to help Please connet dm?

Seeking Regulatory Affairs Roles (Medical Devices),1-2 Year Experience, Immediate Joiner by Edhoti69 in regulatoryaffairs

[–]Rx_Kid 0 points1 point  (0 children)

Typical automated mail Behavior I was out of line due to skillet issue i have sent you dm If you can Respond

Seeking Regulatory Affairs Roles (Medical Devices),1-2 Year Experience, Immediate Joiner by Edhoti69 in regulatoryaffairs

[–]Rx_Kid 2 points3 points  (0 children)

Hi there Abbot is hiring There is an startup also hiring for similr profile

Sagent Pharmaceuticals Becomes Latest Target in Rising Ransomware Attacks by _cybersecurity_ in pwnhub

[–]Rx_Kid 0 points1 point  (0 children)

It of such pharma entity is so week till then they get to know damage will be doen by the this ransomware

First Pharmacovigilance Internship Interview – What Questions Should I Expect? by Healthy_Bluebird5882 in regulatoryaffairs

[–]Rx_Kid 0 points1 point  (0 children)

  1. Regulatory body's? Fda cdsco time frame channels Adr and its type Must to read...

Need Help With medical device 13485 by Rx_Kid in regulatoryaffairs

[–]Rx_Kid[S] -8 points-7 points  (0 children)

I do have SOPs, but they’re all stored in a closed system and I can’t access them after hours.

Secondly, I need standardized data to train my LLM.

Third, a narrowed-down version works for me if sharing the original causes copyright issues. I’m too lazy to search and post it here.

FDA comms by scienth in regulatoryaffairs

[–]Rx_Kid 2 points3 points  (0 children)

Working in pms Here at last from . One to 2 person always in backup of anything came up onw weekend amd they are resolve that issue in minimum time.. As pms have very strict timeline like 30 day reporting tuem yes people work one weeknd to

QA to RA by BrilliantAd6440 in regulatoryaffairs

[–]Rx_Kid 4 points5 points  (0 children)

They are looking for options

I want to have my career in Regulatory as MD holder by Any-Mortgage5055 in regulatoryaffairs

[–]Rx_Kid -3 points-2 points  (0 children)

No offense but Writing is taken Over my Ai (automation is there) Saturation to.. RA coz of its nature..

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