Whether or not you’re from the products setting up, advancement or pharmaceutical lifecycle management phase or require a remediation technique for any compliance disaster, Regulatory Compliance Associates will information you through each pharmaceutical consulting phase on the regulatory process.
Our crew of gurus has successfully carried out quite a few gap analyses in over the last 20 years and delivers this consulting support for all GMP methods.
- When report wanted on urgent basis to assistance the provision, regulatory submissions and so on., When producing web page can’t accommodate the audit as a consequence of chaotic routine, When vacation restriction; Sponsor may get benefits by getting our IGAP experiences from our report databases, In addition our customers only shell out a little portion of the costs normally linked to conducting a supplier audit.
Zero Accident: The potential risk of falling, risks relevant to electricity or managing of machinery, highway hazards, plus much more. Every day, the attention of every and every worker is important to avoid incidents within the office and to stop occupational illnesses.
At Regulatory Compliance Associates, we offer the pharma consulting encounter and pharma consultants essential to guidebook you throughout the quality compliance approach.
Regulatory Compliance Associates Good quality consulting involves assessments, technique, implementations, personnel augmentations, and identification of quality metrics to be certain continuous enhancement. Our pharma consultants have an understanding of the strategic thinking needed to align your business requirements and objectives.
From R&D to supply chain and operations to each side of commercialization, pharma and biotech companies must execute flawlessly across all dimensions if they hope to win.
Company Placing tactics for progress via restructuring, performance enhancements and scaling up of operations.
Nonetheless complicated your daily life sciences source chain, our seasoned industry experts are below that can assist you obtain and preserve finish-to-conclude GMP compliance consistent with present and emerging laws.
Offering a strategic mixture of market acumen, global compliance, and therapeutic knowledge to aid make certain that your progressive Tips aren’t hindered by confined sources.
As the industry grows even larger and aggressive, the war for top quality expertise is getting momentum. This requires Skilled know-how in identifying, sourcing and engaging potential-All set talent.
Developing IQVIA’s positions on crucial tendencies inside the pharma and existence sciences industries, with a focus on EMEA.
On-contact actual-time help through your GMP audit and ongoing assist once the audit until finally you will be more info certified, regardless of what.
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