Laura with Kellerman Consulting is just fantastic. She is quite practical, simple to work with and obtained us by our GMP audit with a much better score than we anticipated. Also, the Firm of many of the files Kellerman Consulting offered us with is superb.
Together with our customers, we use a combination of industry, information, analytical and know-how skills to establish approach advancements that assist you in attaining worth from technological innovation investments.
GMP refers into a set of legal guidelines, benchmarks, and recommendations that relate to the processing of drug substances and merchandise, clinical equipment, in vivo As well as in vitro healthcare merchandise categories, and foodstuff solutions.
Much more not long ago now often called Pharmaceutical Quality Method (PQS), PharmOut features services and merchandise in the form of Expert technological writers and document templates all targeted at offering and powerful and compliant QMS for your website.
Our devoted project management team performs intently using your Management staff to establish and keep track of venture milestones, routine actions, information resources, and report on good results.
A different breed of therapies is coming into clinical progress. Make certain that your approach to drug growth is as modern since the compound you want to convey to market.
Determine the gaps in just your organization’s present Management Technique to be able to fulfil the top practices established by the international benchmarks.
IQVIA Decentralized Trials produce reason-built clinical products and services and systems that engage the appropriate sufferers anywhere they are. Our hybrid and totally virtual methods are already utilised much more than any Some others.
Our groups have many years of encounter in reagent progress and IVD-certified manufacture, as well as a demonstrated reputation creating GMP-quality ancillary reagents for mobile therapy shoppers.
Our services are backed by a Total Quality Assurance. If for virtually any reason, you will be dissatisfied with any company, We'll supply you with a full refund.
Our top quality, producing, CAPA, and provider excellent industry experts conduct extensive process assessments and analyses to make sure all compliance gaps are shut no matter exactly where They might be.
Regulatory Compliance Associates pharma regulatory consultants will create a comprehensive evidence e book of documented proof demonstrating the corrective motion taken to remediate non-compliant issues.
Collectively, we impression everyday living and wellbeing with science. We provide one of the broadest portfolios during the sector for scientists, very best-in-class products for pharmaceutical advancement and read more producing, and a totally built-in assistance Business to help CDMO and GMP consultancy agreement tests throughout standard and novel modalities.
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