Slipstream IT

Not to get ahead of ourselves, but 2025 is going to be a milestone year for our customers migrating to Veeva Vault CRM 👏 → 300+ Successful Veeva Projects → 75+ Veeva CRM Implementations  → 60+ Veeva Vault Implementations  → 100+ Veeva Resources #lifesciences #biotech #slipstream 

When it comes to digital clinical trials, clinical study reports are an essential part of your sNDA submission.  Regulatory medical writers who are experts at creating CSRs for a clinical trial rarely have the experience in real-world data analytics to integrate them effectively into a CSR.   → Where and how does a propensity score and standardized morbidity mortality ratio weighting fit in? → What if you have to bootstrap in order to create confidence intervals, and what if the events of interest are rare? These are the challenges we’ve addressed. → We use your preferred CSR format and modify it to accommodate real-world evidence data and analyses. → We ensure the FDA can review your submission in a structure that feels familiar and is consistent with applicable guidances. CSRs are created, edited, and submitted from a secure and compliant Veeva environment. #lifesciences #biotech #slipstream 

Precision and compliance are non-negotiables in the life sciences.  That means excellence in your PMO matters immensely.  Here’s why: 🔬 Industry Expertise: Biotech and pharma projects aren’t “one size fits all.” A strong PMO understands your regulatory environment, timelines, and critical milestones like sNDAs or clinical trial deadlines. 🛠️ Tailored Processes: A great PMO ensures the right tools (Smartsheet, anyone?) and frameworks are in place to manage the complexity of your projects while staying agile enough to adapt to shifting priorities. 📈 Accountability and Oversight: Clear communication, detailed roadmaps, and transparent tracking mean fewer surprises and more confidence that the project will track to your goals. ⏳ Timely Delivery: When your timelines align with FDA submissions or product launches, delays aren’t an option. A strong PMO keeps things moving with constant communication and management of dependencies. 🤝 Team Alignment: An experienced PMO works as an extension of your team, ensuring alignment across IT, operations, and compliance. Every detail matters. #lifesciences #biotech #slipstream 

🚫 Taking orders 🚫 Reacting to problems 🚫 Fighting unexpected fires ✅ Strategic advisory ✅ Seeing around corners ✅ Taking quick preventative action Get a partner that becomes your eyes & ears. #lifesciences #biotech #slipstream 

As a Veeva Systems Premier Services Partner, our 100+ Veeva consultants are driving more and more transitions to Vault CRM, which we firmly believe to be the next generation CRM for the life sciences. Learn more about the great work Ashwin Girish Kumar & team are doing: https://lnkd.in/gUhKsQwN #lifesciences #biotech #slipstream 

Does this sound familiar? 1 - You hire a new IT service provider, excited for the impact they will make 2 - You’re assigned a junior CSR with little to no life sciences experience 3 - You realize you’ve essentially hired a commoditized IT call center Here’s how we’re the exact opposite: 1 - We reject the traditional call center model and instead operate with “pods” that pair you with 2-3 representatives that are deeply connected to your goals and team. 2 - We’re built exclusively for the life sciences. Our customers range from biotech to pharmaceutical companies as they move through all stages of the product lifecycle. 3 - We’re structured to deliver locally, with global reach. We match your business with our designated local teams, so you always team up with a trusted partner close by. Work with a team that frees you up to focus on your critical mission. #lifesciences #biotech #slipstream 

DATAstream in a nutshell: ✔️ Fully outsourced ✔️ Commercial data ecosystem ✔️ Customizable hub ✔️ Single management platform ✔️ Built exclusively for the life sciences Learn more: https://lnkd.in/guSMtxwu #lifesciences #biotech #slipstream 

What does it *really* take to run a successful digital clinical trial?  It starts with two distinct areas of expertise: 1 - Real-world evidence experts who can wrangle real-world data into actionable insights for external control groups. 2 - Clinical development pros who know how to meet FDA standards and operate within a rigorous framework (like the 250+ SOPs we use at Slipstream). #lifesciences #biotech #slipstream

With DATAstream, we help life science companies pre-align and aggregate all their data to enable a true 360 degree view of the business. Prebuilt analytics are just one of the components our customers love: - OOTB replication for Veeva CRM & Google Analytics - Standard semantic layer views for all Commercial Datasets OOTB - Prebuilt Power BI dashboards for standard Commercial & Digital KPIs Learn more: https://lnkd.in/guSMtxwu

Without Slipstream PMO: Ⓧ Inconsistent project execution Ⓧ Poor transparency into project status Ⓧ Lack of control and insights Ⓧ Delays and overruns With Slipstream PMO: ✓ Project transparency that doesn’t require redundant work ✓ Agile and nimble solutions that enable fast execution ✓ Active management of key business dependencies ✓ Happier teams with fewer headaches and worries Get the organization, processes, and guidance your team needs to end the chaos and do what they do best → https://lnkd.in/dtyfUMk