Validated System Migrations
Change Solutions or Environments While Staying Compliant
Life sciences technology and corporate strategies are changing fast. That means, inevitably, that data will have to move. Of course, the life sciences industry’s rigorous regulatory environment means that’s not quite as simple as it sounds.
When you’re looking to divest an asset or business line, sunset a legacy information management solution or take advantage of a more efficient hosting environment, you need a partner who can get you from here to there with sure-footed confidence. That’s Daelight Solutions.
Our team has years of experience helping pharmaceutical, biotech and medical device companies, as well as CROs and other players in the life sciences ecosystem, plan and execute complex, validated data and content migrations.
We pride ourselves on taking a “big picture” view of each migration and using our proven methodologies to create highly effective migration requirements, testing approaches and workflows. That means less risk and swifter project completions.
A Focus on Compliance
At Daelight, we’re 100% focused on the life sciences industry. We understand all relevant regulations, including Title 21 CFR Part 11’s validation requirements, and know how to keep your content compliant and secure.
General IT consultants might say they know Part 11 and the like, but we’ve lived them for years. Our clients’ success is our success, and in this industry, there’s no success without compliance.
Migrating to Veeva?
Efficiently migrate and validate regulated data and content to Veeva Vault by working with Daelight Solutions, a Veeva Certified Migration Partner.