ProPharma will guide you through the whole Pre-IND approach – from submitting the Preliminary FDA Conference ask for and supporting briefing document by way of planning for and executing the meeting. Our goal is to assist you to meet up with this critical milestone.
What’s much more, we also offer complete and innovative alternatives on your knowledge administration. Your procedures are optimized in numerous means by making use of flexible devices and permit functions to get much more Price tag-successful.
Tap into assorted competencies and skillsets for your predetermined or open up-ended amount of time depending on your evolving requirements.
Enabling you to establish and mitigate the intrinsic possibility in your operations, source chains and company processes.
It is actually effectively explained, with the combination of correct techniques a scientific concept can be transformed into a company acquire.
Unmatched world reach means we can easily function with you to organize your promoting purposes (MAA or NDA) in parallel, preserving you time and cash
With permanent placement through the FDA Team, you could attain 3 Most important objectives: lower the price of talent identification and supply, obtain the confirmed excellent of latest hires, and mitigate the dangers of recruiting new staff.
We’ll use our substantial regulatory and scientific encounter participating With all the FDA to improve the submission method. We provide consulting products and services for critical FDA regulatory submissions, such as:
Some manufacturers could take into consideration testing and certification an impediment to overcome to have to sector. Many others may possibly see it as an important way get more info to cut back chance or liability.
In contrast to a traditional staffing company, our recruiters are material experts who assure Just about every of our means supplies the understanding and abilities you need. We provide superior expertise, speedier and much more Value-properly than common search firms.
A different undertaking for Pharma Consultants is Pharmacovigilance that is definitely relatable to the gathering, detection, assessment, monitoring, and avoidance of adverse outcomes with biologicals, In addition they get the job done read more in the area of resolving contamination issues.
Obtain major cGMP expertise at each and every stage in the item lifecycle. We assistance lifetime science companies quickly access the field's greatest consultants, contractors, and candidates. Our assets support in cGMP, GLP, and GCP compliance across every impacted stage in the product or service lifecycle.
Previously, pharma’s participation in this Room has transpired in fits and commences, yielding few new remedies at scale. To ensure the outcomes they seek right now, pharmaceutical firm leaders initially should coalesce all over and make clear their digital wellness procedures.
As the whole world's major inspection pro, we build methods for the pharmaceutical and biotech industries. Our variety of products and solutions extends from higher-functionality devices and semi-computerized equipment to laboratory models and inspection purposes for in-process control.