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| Certification Vendor: | Salesforce |
|---|---|
| Exam Name: | Salesforce Certified Agentforce Life Sciences Consultant Exam |
| Exam Number: | ALS-Con-201 |
| Passing Score: | 62% |
| Related Certifications: | Salesforce Certified Agentforce Specialist Salesforce Certified Data 360 Consultant Salesforce Certified Platform Administrator |
| Real Exam Qty: | 60 scored questions + up to 5 unscored questions |
| Exam Duration: | 105 minutes |
| Exam Format: | Multiple-choice, Scenario-based questions, Multiple-select |
| Exam Price: | USD 200 (plus applicable taxes) |
| Available Languages: | English |
| Recommended Training: | Life Sciences Cloud Customer Engagement Training Agentforce Life Sciences Consultant Trailhead Path |
| Exam Registration: | Schedule Salesforce Certification Exam Salesforce Certification Exam Registration |
| Sample Questions: | Salesforce ALS-Con-201 Sample Questions |
| Exam Way: | Online proctored or onsite testing center |
| Pre Condition: | Salesforce recommends experience as a Salesforce Consultant, Architect, Developer, or Business Analyst, plus familiarity with life sciences industry processes. Salesforce Certified Platform Administrator is a required prerequisite. |
| Official Syllabus URL: | https://help.salesforce.com/s/articleView?id=005305357&type=1 |
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NEW QUESTION # 95
Choose 1 option.
An Agentforce Life Sciences Consultant has configured the Medical Inquiry process for Cumulus Pharma. When a field sales rep submits a signed inquiry, the status correctly updates to "Submitted," but the Case record remains owned by the rep instead of being automatically routed to the Medical Science Liaisons (MSLs).
Which trigger handler is inactive?
Answer: A
Explanation:
The correct answer is A because the symptom is specifically about Case ownership not changing after a Medical Inquiry is submitted. Salesforce Help for Medical Inquiries shows that the inquiry workflow uses Case status values such as Draft, Signed, Submitted, and Assigned, and Life Sciences Cloud also provides Trigger Handler Administration for configuring Life Sciences trigger handlers, including trigger handlers related to Case objects.
In the scenario, the status update is working correctly: the signed inquiry becomes Submitted. That means the submission process itself is functioning. The failure is isolated to ownership routing: the Case remains owned by the field sales rep instead of being routed to the Medical Science Liaison team or queue. Based on the available options, CaseChangeOwnershipHandler is the handler that directly corresponds to changing ownership on the Case record.
Option B, MSLInquirySubmissionHandler, sounds related to Medical Inquiry submission, but the submission status already updates correctly, so that is unlikely to be the inactive piece. Option C, CaseMSLQueueHandler, sounds like queue routing, but the Salesforce-style handler name that most directly describes the failed behavior is CaseChangeOwnershipHandler. Since the issue is ownership transfer after submission, the inactive trigger handler is CaseChangeOwnershipHandler.
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NEW QUESTION # 96
Choose 1 option.
Cumulus Pharma wants to customize the provider summary to include additional information stored in Agentforce Life Sciences for Customer Engagement. An Agentforce Life Sciences Consultant updated the Actionable Relationship Center (ARC) graph used in provider summarization to include additional objects and fields.
How should the consultant ensure that Provider Summary Generation uses the new information to meet business goals?
Answer: C
Explanation:
The correct answer is A because provider summary generation depends on the prompt template and the data supplied to that prompt. In Life Sciences Cloud account summarization, Salesforce documentation references custom prompt templates for account summarization and the account summarization workflow, while the workflow uses the Generate Provider Account Territory Summary flow as part of the summary-generation process. Salesforce also documents that this flow calls actions such as Get Object Relationship Data and Get Life Sciences Configuration Field Names, meaning the flow participates in retrieving relationship-based data, but the generated business summary still needs the prompt template to know what information to use and how to summarize it.
Updating the ARC graph alone makes additional objects and fields available in the relationship structure, but it does not automatically change the prompt's summarization behavior. To ensure the new information is used correctly, the consultant should create a new prompt template version, update the input dataset so the new fields are included, revise the summarization instructions so the AI knows how to use them, and then activate that version. This aligns with Salesforce's guidance that prompt-based generation relies on the configured prompt and its grounding/input data. Option B is incomplete because changing only the flow does not update the prompt's instructions. Option C is also incorrect because batch-job configuration controls bulk execution, not the actual summarization logic.
NEW QUESTION # 97
Choose 1 option.
A field sales rep is ready to capture a Healthcare Provider's (HCP's) signature on an iPad for a sample drop-off. For Food and Drug Administration (FDA) 21 CFR Part 11 compliance, the system must capture the image of the signature and create a non-editable audit trail linking the signature to the specific samples and timestamp.
Which Agentforce Life Sciences for Customer Engagement feature should an Agentforce Life Sciences Consultant enable to support this rigorous audit requirement?
Answer: A
Explanation:
The correct answer is C because Salesforce's electronic signature capability for Life Sciences is Digital Verification. Salesforce Help states that the Electronic Signature feature provides 21 CFR Part 11-ready electronic signature functionality, and the setup guidance directs administrators to configure the Digital Verifications feature to manage electronic signatures in Salesforce rather than relying on a third-party application.
The requirement is specific to regulated sample drop-off. The system must capture the HCP's signature image, associate it with the sample disbursement, preserve the timestamp, and maintain an audit trail that supports compliance expectations. Digital Verification is the Salesforce Life Sciences feature designed to support electronic-signature capture in this type of regulated workflow.
Option A, Shield Audit Trail, is incorrect because Salesforce Shield can help with broader platform security, event monitoring, and auditability, but it is not the Life Sciences feature that captures an HCP's electronic signature for sample drop-off. Option B, DocuSign for Salesforce, is also incorrect because the question asks for the Agentforce Life Sciences for Customer Engagement feature that supports this requirement. Salesforce Help specifically points to Digital Verification for managing electronic signatures directly in Salesforce. Therefore, the consultant should enable Digital Verification to support the 21 CFR Part 11-ready signature and audit requirements.
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NEW QUESTION # 98
Choose 1 option.
Cumulus Pharma is implementing a feature where Healthcare Providers (HCPs) sign for drug samples on an iPad. The company's compliance team states that, to meet Food and Drug Administration (FDA) 21 CFR Part 11 requirements, a simple image of the signature is insufficient; the system must link the signature to the data and the user's credentials at the exact moment of signing.
Which feature generates this tamper-evident audit trail?
Answer: B
Explanation:
Digital Verification is the correct answer because Salesforce Life Sciences resources describe it as the native capability used to manage electronic signatures in Salesforce and support an organization's 21 CFR Part 11 compliance requirements. Salesforce Help states that Electronic Signatures can be set up using the Digital Verifications feature, allowing signatures to be managed in Salesforce instead of relying on a third-party application. It also references creating a "signature trail," which is the key concept in this question: the signature is not just a stored image, but part of a controlled verification process tied to the signed record and signer context.
Field Audit Trail is not the best answer because it tracks field history and retention for data changes; it does not provide the electronic-signature process required for HCP sample acknowledgments. Adobe Sign is also not the best answer because the question asks for the Salesforce Life Sciences feature that generates the audit trail inside the Life Sciences process. The Salesforce Developer Guide also identifies Digital Verification standard objects as part of the electronic-signature data model, reinforcing that Digital Verification is the Life Sciences capability designed for this use case.
NEW QUESTION # 99
Choose 1 option.
Cumulus Pharma wants to allocate samples from a specific production batch to a field sales rep's inventory so the company can track the remaining quantity by batch and automatically update inventory during disbursements.
Which action fulfills this requirement?
Answer: B
Explanation:
Option C is correct because Product Batch Item is the Salesforce Life Sciences Cloud record that connects a production batch to a specific product inventory location or user inventory context. Salesforce Help describes creating Product Batch Items for sample inventory and states that a product batch item establishes the relationship between the Product, Life Science Marketable Product, Production Batch, Product Batch Item, Location, and User. This directly matches the scenario: Cumulus Pharma needs to allocate samples from a specific production batch to a field sales rep's inventory and track remaining quantity at the batch level.
The ProductBatchItem object also includes the RemainingQuantity field, which supports the requirement to track remaining quantity by batch. Salesforce's Life Sciences Cloud Developer Guide documents ProductBatchItem and identifies RemainingQuantity as a field on the object.
Option A is incorrect because simply assigning a Production Batch to the Life Sciences Marketable Product does not allocate batch-specific stock to a rep's inventory. Visit submissions can update inventory, but the batch allocation must already be represented correctly. Option B is also incorrect because updating Quantity on Hand on Product Item only changes general product inventory at a location. It does not establish the production-batch relationship needed for batch-level tracking. Therefore, the consultant should create a Product Batch Item, associate it to the rep's Product Item, mark it Active, and enter the Remaining Quantity.
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NEW QUESTION # 100
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