s3k Global: Divorce with Peace and Dignity


s3k Global presents:
Divorce with Dignity: Peace of Mind
Thoughtful mediation for a fair, faster, and more private resolution
At s3k Global, we know divorce is deeply personal. Our certified family mediators guide you through every step with compassion and clarity—helping you reach durable agreements on parenting, finances, and property without escalating conflict. We focus on dignity, privacy, and practical outcomes so you can move forward with confidence.
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Certified family mediators with advanced training
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Transparent, flat-fee options
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Virtual and in‑person sessions
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Culturally sensitive and trauma‑informed approach
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Confidential, court‑ready agreements
How Mediation Works
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Free consult (15 minutes): Understand your goals and fit for mediation.
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Intake & safety screening: Ensure a safe, appropriate process for all.
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Guided sessions: Structured conversations to resolve parenting plans, assets, and support.
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Drafting & review: We prepare clear, court‑ready agreements for attorney/party review.
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Filing support: Guidance through the filing process as needed.
What You Can Resolve
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Parenting plans and schedules
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Child and spousal support
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Property and debt division
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Communication and co‑parenting protocols
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Temporary agreements while the case is pending
Why s3k Global
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Neutral, solution‑oriented facilitation
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Respectful, time‑efficient sessions
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Clear timelines and pricing before you begin
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Private, judgment‑free environment
Pricing
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Flat-fee packages and hourly options available.
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Call/Email


Enhancing Healthcare Compliance, Dispute and Conflicts Resolution: HIPPA, High-Risk Areas and Quality Assurance
Clinical Development, Drug Safety and Pharmacovigilance, Medical Devices
All this needs expertise that matters most...
s3kGlobal is more than just about Healthcare Compliance, dispute resolution, negotiations, mediation, ethical settlements, conflict resolution, clinical trial design and intelligent clinical trials.
We specialize in clinical development, medical monitoring, medical affairs, drug and medical device safety and pharmacovigilance in oncology, musculoskeletal, hepatic, neurology and body clinical trials
We concentrate, from the initiation to close out, with an excellence in drug safety and operations, with a holistic production and review of the protocol’s objectives, endpoints, and statistical plan and real world evidence.
How can we achieve accelerated results?
Based on many years of hundreds of clinical trials, we take pride in our trial experts to deliver the best in industry standards that meet compliance and regulatory standard to deliver accelerated and strategic trials.
We minimize adjudication between readers as we believe we can do our home work correctly before even a project begins. We minimize on the costs of a clinical trials by using good clinical practices GCP,GMP.
We are a team of highly trained and experienced physicians, medical professionals in pharmaceuticals and medical device, radiology clinical trials, medical education and product managers.
Our mission is to provide high-quality, innovative and affordable solutions that transform drug development, medical devices, product management, Lean Six Sigma by quality training and skilled and experienced expertise.

Clinical Trials on
Oncology, Neurology, Immunology, Rheumatology
Imaging clinical Trials
Radiology and Imaging Clinical trials-tumors, Lung, Liver, G.I.
Musculoskeletal and other systems of body
Medical Devices
PTDs(Prescription Therapeutic Devices)
Product Management


s3k Global
Efficiency with excellence
A Lean Six Sigma Company



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s3k Global's initiative:
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Regulatory Compliance
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pharmaceutical
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medical devices,
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Medical Monitoring
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Quality and Risk
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Drug and device safety
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Pharmacovigilance
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Clinical Data management
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HIPPA
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site management solutions
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Product management
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Journal publications
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Medical Education
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Conferences
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Webinars
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Ethical Solutions
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Go-No Go Approach
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Career Growth
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Grow Your Clinical Trial Efficiency
Faster, more reliable, drug development, medical devices, medical affairs, medical monitoring, drug safety, pharmacovigilance, regulations and data management from Phase I-IV


