Question 1

What exactly do I get with a Nysom360 subscription?

Accepted Answer

You receive curated intelligence briefs that analyze FDA regulatory developments. Each brief includes an executive summary, detailed analysis, operational impact assessment across functions (Regulatory, Quality, Legal, Executive), and cited sources. Professional subscribers also get full archive access and custom briefing requests.

Question 2

How often are new intelligence briefs published?

Accepted Answer

We typically publish 2-4 briefs per week, depending on FDA activity. Major guidance releases, enforcement actions, or policy shifts are covered within 24-48 hours. Subscribers receive email alerts when new briefs are published.

Question 3

Is this legal or regulatory advice?

Accepted Answer

No. Nysom360 provides regulatory intelligence—analysis and interpretation of public FDA information to inform your decision-making. We do not provide legal, regulatory, or compliance advice. Always consult qualified professionals for specific guidance.

Question 4

What sources do you use?

Accepted Answer

We exclusively use primary FDA sources: Federal Register notices, FDA guidance documents, warning letters, inspection databases, press releases, and official agency communications. We never rely on secondary sources or unverified information.

Question 5

What is the difference between Starter and Professional plans?

Accepted Answer

Starter ($97/month) gives you access to briefs from the last 30 days. Professional ($497/month) includes full archive access, custom briefing requests (3-5 day turnaround), and priority alerts for high-impact developments. Annual billing saves 2 months on both plans.

Question 6

Can I cancel anytime?

Accepted Answer

Yes. There are no long-term contracts. You can cancel your subscription at any time through your account settings. You'll retain access until the end of your current billing period.

Question 7

Do you offer team or enterprise pricing?

Accepted Answer

Yes. For organizations needing multiple seats or custom arrangements, please contact us at intel@nysom360.com to discuss enterprise options.

Question 8

Is there a free trial?

Accepted Answer

We don't offer a free trial, but you can review a complete sample brief on our website to see exactly what you'll receive. This gives you full transparency into our format and depth of analysis.

Question 9

What can I request in a custom briefing?

Accepted Answer

Professional subscribers can request analysis on specific FDA guidance documents, enforcement actions, emerging regulatory themes, or industry-specific implications. Requests are scoped for public information and delivered within 3-5 business days.

Question 10

How many custom briefing requests can I make?

Accepted Answer

Professional subscribers can submit unlimited requests, though we recommend prioritizing your most important topics. Complex requests may require clarification to ensure we deliver exactly what you need.

Question 11

What's NOT included in custom briefings?

Accepted Answer

Custom briefings do not include legal advice, regulatory strategy recommendations, document review, or analysis of confidential/proprietary information. We analyze public FDA information only.

Question 12

How do I access my briefs?

Accepted Answer

After subscribing, you'll have access to a secure dashboard where all briefs are available. You'll also receive email notifications when new briefs are published. Briefs can be bookmarked and searched.

Question 13

Can I share briefs with my team?

Accepted Answer

Your subscription is for individual use. For team access, please contact us about enterprise pricing. Briefs should not be redistributed outside your organization.

Question 14

What if I find an error in a brief?

Accepted Answer

We take accuracy seriously. If you identify an error, please contact us immediately at intel@nysom360.com. We will review, correct if necessary, and note any corrections transparently.

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